JP5124274B2 - Method and apparatus for grasping and evaluating tissue - Google Patents

Abstract

Devices, systems and methods are provided for stabilizing and grasping tissues such as valve leaflets, assessing the grasp of these tissues, approximating and fixating the tissues, and assessing the fixation of the tissues to treat cardiac valve regurgitation, particularly mitral valve regurgitation.

Description

  The present invention relates generally to medical methods, devices, and systems. In particular, the present invention relates to methods, devices and systems for intravascular, percutaneous or minimally invasive surgical treatment of body tissue such as tissue access or valve repair. More particularly, the present invention relates to heart valve and venous valve repair.

  Body surgical repair often involves accessing the tissue and retaining such tissue in an access configuration. In repairing the valve, access to the tissue includes joining the valve leaflets in a therapeutic configuration, where the therapeutic configuration can be maintained by fastening or securing the valve leaflets. . Such a junction can be used to treat blood reflux that most commonly occurs in mitral valves.

  Mitral valve blood regurgitation is characterized by a retrograde flow from the left ventricle of the heart through the malfunctioning mitral valve into the left atrium. During the normal cycle of heart contraction, the mitral valve acts as a check valve to prevent oxygenated blood from flowing into the left atrium. Thus, oxygen-supplied blood is pumped through the aortic valve to the aorta. Valve blood regurgitation significantly reduces heart pumping efficiency and exposes the patient to severe progressive heart dysfunction.

  Mitral blood regurgitation results from many mechanical defects in the mitral valve or left ventricular wall. The valve leaflets, the chords of the valves connecting the leaflets to the papillary muscles, the papillary muscles or the walls of the left ventricle may be damaged or otherwise fail. In general, the annulus can be damaged, inflated, or weakened by the valve, limiting the ability of the mitral valve to close properly against high left ventricular pressure.

  The most common treatment for mitral blood regurgitation relies on valve replacement or repair, including remodeling of the valve and annulus, commonly referred to as annuloplasty. Recent techniques for repairing mitral valves that rely on stitching of adjacent portions of the valve leaflets of the opposite valve are referred to as “bow tie” or “edge-to-edge” techniques. Although all of these techniques can be very effective, these techniques typically rely on open heart surgery, in which the patient's chest is typically opened through a sternotomy and a cardiopulmonary bypass is performed on the patient. The need to open the chest and give the patient cardiopulmonary bypass is traumatic and is associated with high mortality and morbidity associated with it.

  As a result, other additional methods, devices, and systems have been developed for performing mitral and other heart valve repairs. Such methods, devices and systems preferably do not require incisional chest access and use a device that is advanced intravascularly, ie, from a location in the patient's vasculature far from the heart to the heart, or minimally. Can be done by invasive approaches. Examples of such methods, apparatus and systems are described in U.S. Patent Nos. 6,629,534, 6,752,813 and U.S. Patent Application Nos. 10 / 441,753, 10 / 441,531, 11/130818. 10/441508, 11/441687, 10/975555, all of which are incorporated herein by reference for all purposes.

  However, in some cases, various challenges are encountered in desirably securing the valve leaflets. For example, in the case of mitral blood regurgitation, it is generally seen that a portion of the valve leaf moves and shifts out of phase with other leaflets or portions of the leaflets. This occurs due to the elongation or breakage of the structure (the chordae) that holds the leaflets stably and synchronously. Such dysfunction may cause one valve leaflet or part of the leaflet to rock or “sway” above the height of a healthy joint, thereby causing blood to flow back into the right atrium. turn into. Such shaking presents a problem for the practitioner particularly when trying to fix the valve leaf together by the endoscopic approach. The leaflets may be difficult to grip, and even if gripped, the leaflets may not be desirably gripped. For example, the valve membrane may be only partially gripped rather than in full contact with the gripping element. This results in a less desirable bond of the valve membrane, which will eventually dislodge.

  Accordingly, devices, systems, and methods that stabilize tissue to prevent shaking and other movement before and / or during tissue grasping are desirable. In addition, the device that helps to grasp the tissue, allows for a more desirable joining of the tissue, makes an assessment of the grasp, and allows the practitioner to determine whether the desired grasp of the tissue has occurred, particularly prior to fixation. Systems and methods are desired. In addition, devices, systems and methods are desired that allow for the assessment of fixation so that the practitioner can determine whether the desired grasp of tissue has occurred. These devices, systems and methods are useful for the repair of tissues in the body other than the valve leaflets and other than the heart valves. At least some of these objectives are met by the invention described below.

  The present invention relates to various devices, systems and methods for stabilizing, grasping, evaluating and securing tissue, particularly valve leaflets, in the treatment of heart valve blood reflux, and more particularly mitral valve blood reflux. I will provide a. Many of these devices, systems and methods utilize preferred embodiments of a fixation device having at least one proximal element and at least one distal element between which tissue is grasped, or this preferred Used in connection with the embodiment. However, it will be appreciated that the devices, systems and methods of the present invention may utilize any suitable device, particularly any minimally invasive device. When treating the valve leaflets, typically position the fixation device along the joint line at a location that reduces stool blood reflux, such as near the center of the valve, to simulate standard surgical bowtie repair. Grip the valve membrane. However, as discussed in later paragraphs, more than one fixation device may be installed in various arrangements.

  Various devices and techniques are provided to stabilize the tissue prior to grasping to assist in the desired grasping of the tissue. Such stabilization aims to help grasp tissue effectively and efficiently, thereby increasing the likelihood that a desired amount of tissue will be incorporated into the fixation device without requiring multiple grasps. Is. In addition, various devices and techniques are provided to improve grasping, for example, by adjusting the position of the grasped tissue between the proximal and distal elements. Once the tissue or valvular is grasped, it is often desirable to assess the quality of the grasp, such as the amount captured, the orientation of the tissue and the likelihood that the fixation device will maintain the grasp over time. Thus, various devices and techniques are presented for assessing grip quality. Furthermore, once the tissue is fixed by a fixation device, the quality of tissue fixation can be assessed. This can be accomplished by evaluating an improvement in the medical condition being treated, such as an improvement in blood reflux. It is often desirable to evaluate the fixation before delivering and separating the fixation device from the catheter so that the fixation device is repositioned if the improvement is not satisfactory. Thus, various devices and techniques are provided for evaluating fixation before separating the fixation device. Additional devices, systems and methods are also provided.

  In one aspect of the invention, a method is provided for evaluating the grasping of one or more tissues by a minimally invasive device. In one embodiment, the method advances a minimally invasive device having a proximal element and a distal element into a body having tissue into a cavity and the tissue is moved to a proximal element and a distal element. And assessing the presence of tissue in the target area between the proximal and distal elements. Typically, the tissue consists of the valve leaflets. In some embodiments, the presence assessment consists of observing the target area based on fluoroscopy, ultrasound or echocardiography. In such cases, the method further comprises increasing the visibility of at least a portion of the proximal element and / or the distal element. As a modification, or in addition, the method may further comprise increasing the visibility of the tissue.

  In various embodiments, the device has an indicator that indicates the presence of tissue within the target area. In such cases, the method may further comprise observing the indicator. If the indicator changes shape and / or orientation based on the presence of tissue in the target area, observing the indicator includes observing changes in shape and / or orientation.

  In some embodiments, the device has an injectable high visibility material. In such a case, the assessment of the presence of tissue in the target area may consist of observing a highly visible flow pattern of the material. If the substance is contained in a reservoir having a port, the assessment of the presence of tissue in the target area may consist of observing the substance flowing through the port near the target area.

  In a further embodiment, the method further comprises introducing a highly visible substance that can be injected through the device. In such a case, the assessment of the presence of tissue in the target area may consist of observing a highly visible flow pattern of the material. In yet another embodiment, the method further comprises advancing the probe into the target area. In such a case, the assessment of the presence of tissue in the target area may consist of determining the advance depth of the probe. In some embodiments, the apparatus includes a sensor that indicates the presence of tissue within the target area, where the method further comprises evaluating a signal from the sensor.

  In another aspect of the invention, a method is provided for adjusting tissue grasped between proximal and distal elements. In some embodiments, the method includes advancing a minimally invasive device having a proximal element and a distal element into a body cavity having tissue, and moving the tissue distally and distally. Gripping between the elements and adjusting the tissue between the proximal and distal elements. The adjustment may consist of applying suction to the tissue and moving the tissue by suction. If the device has a secondary grasper, the adjustment may consist of grasping and moving the tissue with the secondary grasper. If the device has a rotating component that moves tissue between the proximal and distal elements, the adjustment may consist of rotating the rotating component. If the proximal element is movable relative to the distal element, the adjustment may consist of moving the proximal element relative to the distal element.

  In another aspect of the invention, a method is provided for temporarily stabilizing a valve leaflet. In some embodiments, the method temporarily advances the valve leaflet by advancing a minimally invasive device into a heart chamber having a valve with a valve leaflet and reducing movement into the valve leaflet. Stabilization. If the chamber consists of the left atrium, the valve consists of a mitral valve, the device has a stabilizer, and temporary stabilization consists of positioning the stabilizer on the atrial side of the leaflet so as to reduce valvular sway. It's okay. In some embodiments, the stabilizer comprises an expandable member, a flap or at least one loop. If the device has at least one loop, temporary stabilization may consist of positioning at least one loop in the leaflet to reduce leaflet movement. In some embodiments, the temporary stabilization further comprises moving the at least one loop along the leaflet toward the center of the valve to reduce leaflet movement. If the chamber consists of a ventricle with a chord that extends to the valve leaflets, temporary stabilization may consist of holding the chordae with the device to reduce movement of the valve leaflets. If the device has an expandable member, retention of the chords may consist of expanding the expandable member and hitting the chordae. In some embodiments, temporary stabilization of the valve leaflets comprises temporarily slowing the heart's natural beat with a pacing device.

  In a further aspect of the invention, between at least one proximal element and at least one distal element configured for grasping tissue therebetween, between at least one proximal element and at least one distal element. A minimally invasive device is provided that includes an indicator that indicates the presence of tissue in the target area. In some embodiments, the indicator comprises a high visibility material. For example, the high visibility material may be disposed on or in at least one proximal element and / or at least one distal element. Furthermore, the device may comprise a reservoir in which a highly visible substance is placed. In some embodiments, the reservoir is configured to release at least a portion of the highly visible material due to the presence of tissue in the target region between the at least one proximal and distal elements. Yes. Alternatively or additionally, the reservoir may be configured to move position due to the presence of tissue in the target area between at least one proximal and distal element. Alternatively, the device may comprise a conduit through which highly visible material can be injected through the conduit towards the target area.

  In some embodiments, the indicator is configured to change shape and / or orientation based on the presence of tissue in the target region. For example, the indicator may be configured to extend into the target region in the absence of tissue in the target region and to change the shape or orientation in the target region due to the presence of tissue in the target region. In some cases, the indicator comprises a floating block, flap, reservoir, loop, slack line, probe, detectable element, or any combination thereof.

  In other embodiments, the indicator comprises a sensor. Examples of sensors include conductors, strain gauges, wireless sensors, optical sensors, ultrasonic sensors, magnetic sensors, electrical resistance sensors, infrared sensors, intravascular ultrasonic sensors, pressure sensors, or any combination thereof. As an option, the indicator may be configured to contact the at least one distal element to form a closed circuit when the tissue is not within the target region.

  In another aspect of the invention, between at least one proximal element and at least one distal element configured to grasp tissue therebetween, and between at least one proximal element and at least one distal element. A minimally invasive device is provided that includes an adjustment element configured to adjust a portion of the tissue. In some embodiments, the adjustment element is a vacuum tube configured to apply suction to the tissue to adjust the position of the portion of tissue between the at least one proximal element and the at least one distal element. It consists of a road. In other embodiments, the adjustment element comprises a secondary grasper configured to grasp tissue to adjust a portion of tissue between the at least one proximal element and the at least one distal element. . In still other embodiments, the adjustment element comprises a rotating component configured to move tissue to adjust a portion of tissue between the at least one proximal element and the at least one distal element. In still other embodiments, the adjustment element is configured to adjust the position of the at least one proximal element to move tissue relative to the at least one distal element.

  In a further aspect of the invention, between at least one proximal element and at least one distal element configured for grasping tissue therebetween, between at least one proximal element and at least one distal element. A minimally invasive device is provided that includes a stabilizer configured to reduce tissue movement prior to grasping the tissue. Where the tissue consists of a mitral valve leaflet, the stabilizer comprises an expandable member, flap, overtube or at least one loop configured to be positioned on the atrial side of the valve leaflet to reduce valvular sway. May be. For example, the stabilizer may consist of at least one loop that is movable toward the center of the valve to reduce movement of the valve membrane. If the tissue consists of a valvule from which the chordae extend, the stabilizer may consist of an expandable member configured to hold the chordae during expansion to reduce valvular movement.

  In another aspect of the invention, a fixation device having at least one proximal element and at least one distal element configured for grasping tissue therebetween, a proximal end, a distal end, and a A catheter having a lumen therethrough and configured to be advanced intraluminally through at least a portion of the body to tissue and a shaft removably coupled to the fixation device A system is provided for assessing the quality of tissue fixation in the body. The shaft is configured to pass through the lumen of the catheter, and at least a portion of the shaft is catheterized while tissue is grasped between at least one proximal element and at least one distal element. Flexible to allow movement of the fixation device relative to. In some embodiments, the shaft consists of a compression coil. Thus, the system may further comprise a central actuation wire configured to extend through the compression coil to make the compression coil rigid during installation of the fixation device. As an option, the system may have a sheath that is extensible over at least a portion of the flexible shaft to render the flexible shaft rigid during installation of the fixation device. In this case, such a stiffening element is removed to allow movement of the fixation device while the tissue is grasped to assess the desirability of fixation.

  In another aspect of the present invention, a method is provided for securing the leaflets of a pair of valves together along a joint line. In this method, the valve membranes of the pair of valves are both fixed at a first position along the joint line by the first fixing device, and the valve positions of the pair of valves are both fixed by the second fixing device at the second position along the joint line. And the first and second positions are different. In some embodiments, the first and second positions are adjacent to each other. Alternatively, the first and second positions may be spaced apart, for example, approximately 1 cm apart. The first and second positions are positioned to give a single, double or triple valve port geometry, to name a few examples when opening the valve membrane of a pair of valves due to a pressure gradient. May be.

  In some embodiments, the first fixation device has a first pair of gripping elements and a second pair of gripping elements. Thus, fixing the valve membranes of the pair of valves together in the first position means that one of the valve membranes of the pair of valves is held between the first pair of gripping elements, and the valve membranes of the pair of valves are The other valve membrane may be gripped between the second pair of gripping elements. Further, fixing the valve membranes of the pair of valves together in the second position means that one of the valve membranes of the pair of valves is gripped between the first pair of gripping elements of the second fixing device. The other valve membrane of the valve membrane of this valve may be grasped between the second pair of grasping elements of the second fixing device. In some embodiments, the method further includes after the step of locking the pair of valve membranes together in the first position to determine the necessity of locking the pair of valve membranes together in the second position. Evaluating the performance of the valve leaflets.

  Other objects and advantages of the present invention will become apparent from the following detailed description when taken in conjunction with the accompanying drawings.

  The present invention stabilizes and grasps tissue such as the valve leaflets, evaluates grasping of these tissues, and approaches these tissues to treat heart valve blood regurgitation, particularly mitral blood regurgitation. Devices, systems and methods for fixing them and assessing tissue fixation are provided.

  The grip is preferably atraumatic and provides many advantages. Atraumatic means that the devices and methods of the present invention can be applied to the leaflet and then removed without causing any significant clinical damage to the structure or function of the leaflet. The valve membrane and valve continue to function in substantially the same manner as before the present invention was applied. Thus, while satisfying the definition of “atraumatic”, using the present invention, some slight penetration or indentation of the leaflets can occur. This allows the device of the present invention to be attached to a diseased valve and removed or repositioned if desired without adversely affecting valve function. Also, in some cases, it may be necessary or desirable to pierce the valve membrane during gripping, fixation, or both gripping and fixation, or otherwise permanently affect it. It will be understood that there is. It may also be desirable to incorporate more valvular tissue so that when the leaflets are grasped, the initial grasp results in a firm fixation of the tissue. Further, when the leaflets are grasped, the user is given a reaction result that sufficient leaflets have been taken in and / or the resulting installation instructions prior to releasing the fixation device. Thereby, it may be desirable to allow repositioning or correction of the installation, if desired.

  It will be appreciated that each of the stabilization, grasping, approaching, securing, and evaluation steps may be accomplished by separate devices, or multiple steps may be accomplished by a single device. Let's go. In some embodiments, all of these steps may be accomplished with a single device. Further, in some embodiments, multiple steps are performed by separate devices that approach the tissue from different directions. For example, when treating a mitral valve, some devices may use atrial access and other devices use ventricular access. Many embodiments are performed to achieve these results, but a general summary of the basic features is presented here. Such features are not intended to limit the scope of the invention, but are presented for the purpose of providing a basis for the description of individual embodiments presented later in this application.

I. Overview of the Fixing Device Many of the devices, systems and methods of the present invention are described in the present specification and in US Pat. Nos. 6,629,534 and US patent applications 10 / 441,531 and 11/130818 (all of these). Are used or are used in conjunction with preferred embodiments of the fixation device described in the present disclosure by reference to all purposes. The fixation device is positioned near the desired treatment site and is provided by an interventional tool used to grasp the target tissue. For intravascular applications, the interventional device is typically an interventional catheter. For surgical applications, the interventional tool is typically an interventional instrument. In a preferred embodiment, fixation of the grasped tissue is achieved by maintaining the grasp on the part of the interventional device that is left behind as an implant. The present invention may have a variety of uses for tissue access and tissue fixation throughout the body, but is well suited for valves, particularly heart valves such as mitral valves.

  Referring to FIG. 1A, an interventional device 10 having a delivery device such as a shaft 12 and a fixation device 14 is shown approaching the mitral valve MV from the atrial side and grasping the leaflet LF. Has been. The mitral valve may be accessed surgically or by using endovascular techniques and by retrograde access through the ventricle or by antegrade access through the atria as described above. For illustrative purposes, forward approach is described.

  The fixation device 14 is releasably attached to the shaft 12 of the interventional tool 10 at its distal end. Here, when describing the device of the present invention, “proximal” means the direction towards the end of the device to be manipulated by the user outside the patient's body, and “distal” means the treatment site. Means the direction toward the working end of the device positioned in a direction away from the user. With respect to the mitral valve, proximal refers to the atrial side or upstream side of the valve leaflet, and distal refers to the ventricular side or downstream side of the valve leaflet.

  The fixation device 14 typically includes a proximal element 16 (ie, a gripping element) and a distal element 18 (ie, a fixation element) that project radially outward, and these elements 16, 18. Can be positioned on either side of the leaflet LF as shown to capture and hold the leaflet between them. The proximal element 16 is preferably composed of cobalt chrome, nitinol or stainless steel and the distal element 18 is preferably composed of a cobalt chrome alloy or stainless steel (such as Elgiloy®), Any suitable material may be used. The fixing device 14 can be coupled to the shaft 12 by a coupling mechanism 17. According to the coupling mechanism 17, the fixing device 14 can be removed or left as an implant in order to hold the valve membrane together in the joint position.

  In some situations, it may be desirable to reposition or remove the fixation device 14 after the proximal element 16 and / or the distal element 18 have been deployed to capture the leaflet LF. Such repositioning or removal can achieve good valve function, more optimal positioning of the device 14 in the leaflet, good grip on the leaflet, and, for example, the device 14 can be like chordal tissue. It may be desirable for a variety of reasons, such as untangling from surrounding tissue, replacing the device 14 with a device of a different design, or re-accessing the valve in an attempt to interrupt the fixation procedure. . To facilitate repositioning or removal of the fixation device 14, the distal element 18 can be released without tangling with, interfering with, or damaging the chordal tissue, each valve or other tissue. And optionally reversible to a configuration suitable for withdrawing device 14 from the valve. FIG. 1B shows reversal in which the distal element 18 is movable in the direction of arrow 40 to the reversal position. Similarly, the proximal element 16 may be raised if desired. In the reverse position, the device 14 can be repositioned to the desired orientation, in which the distal element can then be returned to a gripping position that strikes the leaflet as in FIG. 1A. Alternatively, the fixation device 14 can be extracted from the valve membrane (as shown by arrow 42) as shown in FIG. 1C. Such reversal reduces trauma to the valve membrane and minimizes any entanglement of the device with the surrounding tissue. Once the device 14 is withdrawn through the valve leaflets, the proximal and distal elements can be moved to a closed position or configuration suitable for removal from the body or re-insertion into the mitral valve.

  2A-2C show exemplary locations of one or more stationary phases 14 in the desired orientation relative to the leaflet LF. These figures are short axis views of the mitral valve MV from the atrial side, so the proximal element 16 is shown as a solid line and the distal element 18 is shown as a dashed line. The proximal and distal elements 16, 18 are typically positioned to be substantially perpendicular to the bond line C. The device 14 can be moved roughly along the bond line to any desired position for fixation. The leaflet LF is held in place during diastole so that the leaflet LF remains in place between the elements 16, 18 surrounded by the opening O resulting from the diagnostic pressure gradient, as shown in FIGS. 2A-2C. The Advantageously, the leaflets LF are joined such that their proximal or upstream surfaces face each other in a vertical orientation parallel to the direction of blood flow through the mitral valve MV. The upstream surfaces may be brought together in contact with each other or may be held slightly apart but are preferably maintained in a vertical orientation where they face each other at the junction. Referring to FIG. 2A, the dual valve mouth geometry of a standard surgical bowtie repair is simulated by placing the fixation device near the center of the leaflet LF. Color Doppler echo shows whether the valve's blood reflux has been reduced. If the resulting mitral valve flow pattern is satisfactory, the valve leaflets may be secured together in this orientation. If the resulting color Doppler image shows inadequate improvement in mitral valve blood regurgitation, the interventional tool may be repositioned. This should be repeated until an optimal result is produced where the leaflet LF is held in place. Once the leaflets are joined in the desired configuration, the fixation device 14 is removed from the shaft 12 and left behind as an implant to hold the leaflets together in the joining position. As shown in FIGS. 2B-2E, it may be desirable to add an additional securing element 14 ′. In FIG. 2B, an additional anchoring element 14 'is positioned beside the previously installed anchoring element 14 to retain the dual valve port geometry. In FIG. 2C, the additional anchoring element 14 ′ is positioned at a distance such as up to 1 cm from the previously installed anchoring element 14 to produce a triple valve geometry. In FIG. 2D, the fixation elements 14 ′ are positioned adjacent to each other near the first commissure CM1. Such an arrangement generally results in a single valve mouth geometry by pleating on one side of the valve opening. Similarly, as shown in FIG. 2E, one securing element 14 may be positioned near the first commissure CM1, and an additional securing device 14 ′ may be positioned near the second commissure CM1. Such an arrangement also generally results in a single valve mouth geometry by pleating on one side of the valve opening. An additional fixation device 14 ′ may be desired to ensure proper fixation of the leaflet LF and / or to further reposition the leaflet LF. Additional securing devices 14 'may be added at any time during the procedure, or may be added in a separate procedure at a later time. It is possible to position any number of fixation elements 14, including two, three, four, five or more fixation elements 14 to fix the valve membrane or any other tissue You will understand.

  FIG. 3 shows an embodiment of the fixing device 14. In this view, the fixation device 14 is shown coupled to the shaft 12 as the interventional tool 10. The fixation device 14 includes a coupling member 19 and a plurality of opposed distal elements 18. The distal element 18 includes an elongate arm 53, each arm having a proximal end 52 rotatably coupled to the coupling member 19 and a free end 54. The free end 54 has a round shape to minimize interference with the surrounding tissue structure and trauma to the surrounding tissue structure. Preferably, each free end 54 constitutes a curvature around two axes, one of which is the longitudinal axis 66 of the arm 53. Thus, the engagement surface 50 has a surface area that contacts the tissue and has a cup-shaped or concave shape to help grasp and hold the valve leaflets. This further allows the arm 53 to be fitted around the shaft 12 in the closed position to minimize the profile of the device. Preferably, the arms 53 are at least partially cupped or curved inwardly about their longitudinal axis 66. Also preferably, each free end 54 constitutes a curvature about an axis 67 perpendicular to the longitudinal axis 66 of the arm 53. This curve is the reverse curve along the most distal portion of the free end 54. Similarly, the longitudinal edge of the free end 54 may flare outward. Both reverse curvature and flaring minimize trauma to the engaged tissue. Furthermore, the arm 53 has a plurality of openings to increase grip strength and promote tissue ingrowth after implantation.

  The valve leaflet is grasped between the distal element 18 and the proximal element 16. In some embodiments, the proximal element 16 is fixable, elastic, and cantilevered from the coupling member 19. Proximal element 16 is preferably resiliently biased toward the distal element. Each proximal element 16 is shaped and positioned to be at least partially recessed within the recess of the distal element 18 when no tissue is present. When the fixation device 14 is in the open position, the proximal elements 16 are each separated from the engagement surface 50 near the proximal end 52 of the arm 53 and, as shown in FIG. In a state where the free end portion of the contact portion is in contact with the engagement surface 50, the shape is determined so as to be inclined toward the engagement surface 50 near the free end portion 54. This shape of the proximal element 16 accommodates the valve leaflet or other tissue of varying thickness.

  The proximal element 16 may have a plurality of openings 63 and shell-like side behaviors 61 to increase the grip on the tissue. Optionally, the proximal element 16 has a friction appendage, a friction feature or a gripping force enhancing element to help grasp and / or hold the leaflet. In the preferred embodiment, the friction appendage comprises a barb 60 having a tapered pointed tip extending toward the engagement surface 50. Use any suitable friction appendage such as protrusions, windings, bands, barbs, grooves, channels, ridges, surface irregularities, sintered parts, high friction pads, covers, coatings, or combinations thereof It will be appreciated that this is acceptable. As an option, magnets may be present on the proximal and / or distal elements. The mating surface is made of or has a material of opposite magnetic charge to cause attraction by magnetic force. For example, the proximal and distal elements can each be counter-loaded magnetic material such that the tissue is held between the proximal and distal elements to facilitate rapid healing and ingrowth of the tissue. You may have. Also, in addition to or instead of biasing the proximal element toward the distal element, magnetic force may be used to attract the proximal element 16 toward the distal element 18. This can aid in deployment of the proximal element 16. In other examples, the distal elements 18 each have an unloaded magnetic material so that the tissue located between the distal elements is held between them by magnetic force.

  Further, the fixing device 14 has an operation mechanism 58. In this embodiment, the actuation mechanism 58 comprises two link members or legs 68, each leg 68 being pivotally joined to one of the distal elements 18 at a rivet joint 76. 70 and a second end 72 rotatably joined to the stud 74. Legs 68 are preferably constructed of a rigid or semi-rigid metal or polymer such as Elgiloy®, cobalt chrome or stainless steel, although any suitable material may be used. In the illustrated embodiment, both legs 68 are pinned to studs 74 by a single rivet 78, although each leg 68 may be individually attached to stud 74 by a separate rivet or pin. You will understand. The stud 74 can be joined to an actuator rod 64 (not shown) extending through the shaft 12 that moves the stud 74 and thus the legs to place the distal element 18 in the closed position. , Is axially extensible and retractable for rotation between an open position and a reverse position. Similarly, immobilization of the stud 74 holds the leg 68 in place and thus holds the distal element 18 in the desired position. The stud 74 may be locked in place by a locking feature.

  In any of the embodiments of the fixation device 14 disclosed herein, the distal element 18 and the proximal element 16 can be moved or deflected as the valve leaflets are opened or closed, so that they are in the closed position. It may be desirable to provide some mobility or flexibility to the distal element 18 and / or the proximal element 16 at. This provides shock absorption, thereby reducing the force on the leaflet and minimizing the possibility of tearing or other trauma to the leaflet. Such mobility or flexibility may be provided by using a flexible and elastic metal or polymer of appropriate thickness to construct the distal element 18. Also, the locking mechanism of the fixation device (described below) may be constructed of a flexible material to allow some slight movement of the proximal and distal elements even when locked. Further, the distal element 18 is coupled to the coupling mechanism 19 or actuating mechanism 58 by a mechanism that biases it inward (inward) but slightly opens the arm in response to the force exerted by the valve membrane. be able to. For example, rather than being pinned at a single location, these components may be pinned through a slot that allows a small amount of translation of the pin depending on the force on the arm. A spring is used to bias the pinned component toward one end of the slot.

  4A-4B, 5A-5B, 6A-6B, and 7A-7B are views of the fixation device 14 of FIG. An embodiment is shown. FIG. 4A shows an embodiment of the interventional device 10 delivered through the catheter 86. It will be appreciated that the interventional tool 10 may take the form of a catheter, and similarly, the catheter 86 may take the form of a guide catheter or sheath. However, in this example, the words “intervention tool 10” and “catheter 86” are used. The interventional tool 10 includes a fixation device 14 coupled to the shaft 12, which is shown in the closed position. FIG. 4B shows a similar embodiment of the fixation device 14 of FIG. 4A in a larger view. In the closed position, the opposing pair of distal elements 18 are positioned such that the engagement surfaces 50 face each other. Each distal element 18 comprises an elongate arm having a cup-like or concave shape, both of which surround the shaft 12 and, optionally, come into contact with each other on both sides of the shaft. Yes. This provides a low profile of the fixation device 14 that can be easily passed through the catheter 86 and any anatomical structure such as a mitral valve. FIG. 4B further includes an operating mechanism 58. In this embodiment, the actuation mechanism 58 includes two legs 68 that are each movably coupled to a base 69. The base 69 extends through the shaft 12 and is joined to an actuator rod 64 that is used to manipulate the fixation device 14. In some embodiments, the actuator rod 64 is directly attached to the actuation mechanism 58, particularly the base 69. However, as a modification, the actuator rod 64 may be attached to a stud 74 attached to the base 69. In some embodiments, the stud 74 is threaded so that the actuator rod 64 attaches to the stud 74 by a threaded action. However, the rod 64 and stud 74 may be joined by any mechanism that is releasable to remove the fixation device 14 from the shaft 12.

  5A-5B show the fixation device 14 in the open position. In the open position, the distal element 18 is rotated so that the engagement surface 50 is oriented in the first direction. Actuating the actuator rod 64 causes the stud 74 to advance distally relative to the coupling member 19 to apply force to the distal elements 18, which move in the direction of the joint 76 due to the freedom of movement in this direction. Start spinning around. Such rotation and radial outward movement of the distal element 18 causes rotation of the leg 68 around the joint 80 so that the leg 68 is immediately slightly outward. The stud 74 may be advanced to any desired distance that correlates to the desired separation of the distal element 18. In the open position, the engagement surface 50 is disposed at an acute angle with respect to the shaft 12, and is preferably at an angle between 90 and 180 degrees relative to each other. In one embodiment, in the open position, the free end 54 of the arm 53 has a span between both about 10 to 30 mm, usually about 12 to 18 mm, preferably about 14 to 16 mm.

  Proximal element 16 is typically biased outward toward arm 53. Proximal element 16 is moved inward toward shaft 16 and proximal element line 90, which can be in the form of a suture, wire, nitinol wire, rod, cable, polymer line or other suitable structure. May be held against the shaft 12. The proximal element lines 90 may be coupled to the proximal element 16 by passing them in various ways. If the proximal element 16 has a loop shape as shown in FIG. 5A, the line 90 may pass through the loop and back. If the proximal element 16 has an elongated solid shape as shown in FIG. 5B, the line 90 may pass through one or more of the openings 63 in the element 16. Further, as shown in FIG. 5B, a line loop 48 may be present in the proximal element 16 and the proximal element line 90 may pass through this line loop 48 and back. Such a line loop 48 is used to reduce friction against the proximal element line 90, or the proximal element 16 is solid, or lacks other loops or openings through which the proximal element line 90 passes. It may be useful if you are. The detachable means of attaching the single line 90 to the proximal element 16 without reversing or removing the single line 90 directly from the proximal element 16 when desired causes the proximal element line 90 to be approximated. It may be attached to the positioning element 16. Examples of such removable means are hooks, snares, clips or breakable joints, to name a few. By applying sufficient tension to the proximal element line 90, the removable means may be removed from the proximal element 16 by, for example, breaking the joint. Other mechanisms for removal may be used. Similarly, the locking line 92 may be attached to or removed from the locking mechanism by similar removable means.

  In the open position, the fixation device 14 can engage the tissue that is to be approached or treated. This embodiment is adapted for treatment of the mitral valve using antegrade access from the left atrium. The interventional device 10 is advanced through the mitral valve from the left atrium to the left ventricle. The distal element 18 is oriented perpendicular to the bond line and then positioned so that the engagement surface 50 contacts the ventricular surface of the valve leaflet, thereby grasping the leaflet. The proximal element 16 remains on the atrial side of the valve leaflet such that the leaflet is located between the proximal and distal elements. In this embodiment, the proximal element 16 has a friction appendage such as a barb 60 that is directed toward the distal element 18. However, at this point, neither the proximal element 16 nor the barb 60 contacts the valve membrane.

  The interventional tool 10 may be repeatedly manipulated to reposition the fixation device 14 so that the leaflets are properly contacted or gripped at the desired location. Repositioning is accomplished with the fixation device in the open position. In some cases, blood reflux may be suppressed while the device 14 is in the open position. If blood regurgitation is not reduced satisfactorily, the device may be repositioned and blood regurgitation may be inhibited again until the desired result is achieved.

  It may be desirable to reverse the fixation device 14 to assist in repositioning or removal of the fixation device 14. 6A-6B show the fixation device 14 in the reverse position. By further advancing the stud 74 relative to the coupling member 19, the engagement surface 50 faces outward and the free end 54 is distal in a state where each arm 53 forms an obtuse angle with respect to the shaft 12. The distal element 18 is further rotated to point to. The angle between the arms 53 is preferably in the range of about 270 to 360 degrees. Further advancement of the stud 74 further rotates the distal element 18 about the joint 76. This rotation and radially outward movement of the distal element 18 causes the rotation of the legs 68 around the joint 80 so that the legs 68 return to their original positions that are generally parallel to each other. The stud 74 may be advanced to any desired distance that correlates with the desired reversal of the distal element 18. Preferably, in the fully reversed position, the span between the free ends 54 is only about 20 mm, usually less than about 16 mm, preferably about 12-14 mm. In this example, the proximal element 16 remains positioned against the shaft 12 by exerting tension on the proximal element line 90. Thus, a relatively large space can be created between the elements 16, 18 for repositioning. Also, the reverse position allows the fixation device 14 to pass through the valve while minimizing trauma to the valve membrane. The engagement surface 50 provides an atraumatic surface for deflecting tissue when the fixation device is retracted proximally. It should be noted that the barb 60 is slightly tilted in the distal direction (in the direction away from the free end of the proximal element 16) so that when the anchoring device is withdrawn, the barb will catch on or tear the tissue. Reduce fear.

  Once the anchoring device 14 is positioned in the desired position against the valve leaflets, the leaflets can then be captured between the proximal element 16 and the distal element 18. 7A-7B show the fixation device 14 in such a position. Here, the proximal element 16 is lowered toward the engagement surface 50 to retain the leaflets therebetween. In FIG. 7B, the proximal element 16 is shown having a barb 60 that may be used to perform atraumatic grasping of the leaflets. As a modification, a larger, more sharply pointed barb or other intrusion structure may be used to help more actively pierce the leaflet and hold it in place. This position is similar to the open position of FIGS. 5A-5B, but in this case the proximal element 16 is arm 53 by releasing tension on the proximal element line 90 to compress the valvular tissue therebetween. It is descended towards. If the reflux has not been sufficiently reduced in the blood, at any point in time, the proximal element 16 can be raised and the distal element 18 adjusted or reversed to reposition the fixation device 14.

  After the leaflet is captured between the proximal element 16 and the distal element 18 in the desired configuration, the distal element 18 is locked to hold the leaflet in this position, or the fixation device 14 is closed. Or you may go back to it.

  It will be appreciated that the fixation device of the present invention may have any or all of the functions and features described above. For example, the fixing device 14 may or may not be movable to the reverse position. Alternatively, stationary phase 14 may or may not have proximal element 16. Thus, the foregoing aspects of the fixation device 14 are merely preferred embodiments and are not intended to limit the scope of the invention.

II. Stabilization of the leaflets Various devices and techniques are provided to stabilize the leaflets prior to gripping. Such stabilization is aimed at gripping the valve membrane effectively and efficiently, thereby increasing the likelihood that the desired amount of valve membrane will be incorporated into the fixation device without requiring multiple grips. . It will be appreciated that the stabilization devices and techniques may be used in combination with the aforementioned fixation devices, or may be used with any suitable gripping and / or fixation device. Furthermore, many of such stabilization techniques and devices may be used to stabilize the valve leaflets or other tissues for any purpose.

  Typically, in the case of mitral blood regurgitation, a portion of the leaflet LF moves inconsistent with other leaflets or portions of the leaflet. This occurs due to the stretching or cutting of the structure (the chordae) that holds the leaflets stably and synchronously. As a result of such dysfunction, one valve leaflet or part of the leaflet rocks or “sways” above the level of a healthy joint, causing blood to flow back into the right atrium. End up. 8A-8L, 9A-9B, and 10A-B show an apparatus for stabilizing a valve leaflet by reducing the upward movement and swaying of the leaflet in order for the user to more securely grasp the targeted leaflet. An embodiment is shown. In these embodiments, as shown in FIG. 8A, the catheter 86 is advanced into the left atrium LA of the heart H, and the fixation device 14 is advanced through the catheter 86 and the mitral valve MV with the leaflet LF. Thus, a part of the fixing device 14 is positioned in the left ventricle LV. The valve leaflet LF is shown swaying upward toward the left atrium LA while the fixation device 14 is below the valve in the left valve chamber LV. In this example, the fixation device 14 is similar to the fixation device described above with respect to FIG. 3 and has a proximal element 16 and a distal element 18. The fixation device 14 is at least partially open to extend the distal element 18 radially outward while the proximal element 16 remains held on the shaft 12. It is desirable to engage the leaflet LF with the distal element 18 so that the proximal element 16 is lowered to grip the leaflet LF therebetween.

  One or more stabilization loops 100 may be advanced from the catheter 86 and positioned on the atrial side of the leaflet LF. FIG. 8B shows a cross-sectional top view of an embodiment of the stabilization loop 100. The loop 100 is shown extending radially outward from the catheter 86 to form a circular shape. The diameter of the circular shape may be changed by advancing or retracting the loop 100 from the catheter 86. The loop 100 may be composed of any suitable material such as metal, polymer or fiber and may have any suitable form such as wire, ribbon, link or fabric. FIG. 8C shows a side view of the embodiment shown in FIG. 8B. The circular shape of the loop 100 lies in a plane that is substantially perpendicular to the catheter 86. Thus, the loop 100 may be positioned along the valve annulus as shown in FIG. 8A. In this position, the leaflet LF may still sway upward. Referring to FIG. 8D, the diameter of the loop 100 may be reduced as indicated by arrow 102. This may be accomplished by partially retracting the loop 100 into the catheter 86. Due to the continuous decrease in diameter, the loop 100 is drawn from the annulus toward the center of the valve. As the loop 100 moves (the previous loop 100 ′ is indicated by a dashed line), the loop 100 restricts upward movement or swaying of the leaflet LF in a controlled manner and between the proximal element 16 and the distal element 18. The leaflet LF is positioned for grasping.

  There may be more than one loop 100 to stabilize the valve membrane, these loops may be concentric, adjacent to each other, in separate planes, or optional It will be appreciated that any suitable arrangement may be used. For example, FIG. 8E shows an embodiment having a first loop 100a and a second loop 100b. These loops 100a, 100b function similarly to the embodiment shown in FIGS. 8A-8D, but the second loop 100b is smaller and is located concentrically within the first loop 100a. The diameters of the loops 100a and 100b may have any appropriate size, and the relationship between the diameters may change. FIG. 8F shows a side view of the embodiment shown in FIG. 8E. As shown, the circular shape of the loops 100 a, 100 b lies in a plane that is substantially perpendicular to the catheter 86. Thus, in order to stabilize the valve membrane LF, the loops 100a and 100b may be positioned against the valve membrane LF. The diameter of the loops 100a, 100b may then be reduced simultaneously or individually by partially retracting the loops 100a, 100b into the catheter 86. Due to the continuous decrease in diameter, the loops 100a, 100b are drawn toward the center of the valve. Also, as the loops 100a, 100b move, the loops 100a, 100b restrict the upward movement or swaying of the leaflet LF in a controlled manner and for optimal grip between the proximal and distal elements 16,18 Position the LF.

  FIG. 8G shows another embodiment having a first loop 100a and a second loop 100b. However, in this embodiment, the loops 100a, 100b are non-concentric and each loop extends from the opposite side of the catheter 86. The diameters of the loops 100a and 100b may have any appropriate size, and the relationship between the diameters may change. FIG. 8H shows a side view of the embodiment shown in FIG. 8G. As shown, the circular shape of the loops 100 a, 100 b lies in a plane that is substantially perpendicular to the catheter 86. Thus, in order to stabilize the valve membrane LF, the loops 100a and 100b may be positioned against the valve membrane LF. FIG. 8I shows a top view of the mitral valve MV, where the catheter 86 is positioned above the valve MV so that a fixation device (not shown) is passed through the leaflet LF. The loops 100a, 100b are shown extending radially outward toward the annulus. Then, the diameter of the loops 100a, 100b may be reduced as indicated by the arrow 102. This may be achieved by partially retracting the loops 100a, 100b into the catheter 86. Due to the continuous decrease in diameter, the loops 100a, 100b are drawn from the annulus toward the center of the valve. When the loops 100a and 100b move (the previous loops 100a ′ and 100b ′ are indicated by chain lines), the loops 100a and 100b restrict the upward movement or sway of the valve membrane LF by a control method and The leaflet LF is positioned for optimal grasping between the distal and distal elements 16,18. As shown, each loop 100a, 100b limits the movement of individual leaflets LF. However, it will be appreciated that the catheter 86 may be oriented (eg, at a 90 degree rotation) such that each loop 100a, 100b contacts more than one leaflet LF.

  FIG. 8J shows an embodiment having a single loop 100 in a plane substantially parallel to the catheter 86. FIG. 8K shows a side view of the embodiment shown in FIG. 8J. The loop 100 may have any suitable shape and diameter. Thus, the loop 100 may be positioned against the leaflet LF to stabilize the valve leaflet LF. FIG. 8L shows a top view of the mitral valve MV, in which the catheter 86 is positioned over the valve MV so that a fixation device (not shown) is passed through the leaflet LF. The loop 100 is shown extending radially outwardly toward the annulus perpendicular to the commissure C. Such positioning limits the upward movement of the valve membrane LF. Also in this case, the diameter of the loop 100 may be reduced as indicated by the arrow 102. This may be accomplished by partially retracting the loop 100 into the catheter 86. Due to the continuous decrease in diameter, the loop 100 is drawn from the annulus toward the center of the valve. As the loop 100 moves (the previous loop 100 ′ is indicated by a dashed line), the loop 100 maintains limited upward movement or swaying of the leaflet LF and between the proximal and distal elements 16,18. Position the leaflet LF for optimal gripping.

  It will be appreciated that in any of the foregoing embodiments, the loop may be extended to stabilize both valve membranes, or may be extended to stabilize one agitating valve membrane. Will. This may be achieved by orientation of the catheter 86, the shape of the loop 100, the amount of loop 100 extension, or any other method. The embodiment shown in FIGS. 8G-8I is particularly adapted to single valve perturbation, in which case only the first loop 100a may be present. It will further be appreciated that the loop 100 may have a surface treatment or appendage such as a roller or gripper to help stabilize the valve membrane.

  9A-9B illustrate another embodiment that stabilizes the valve leaflet LF by reducing upward movement and swaying of the valve leaflet LF. As shown in FIG. 9A, the catheter 86 is advanced into the atrium LA of the heart H and the fixation device 14 is passed through the catheter 86 and the mitral valve with the leaflet LF so that at least the fixation device 14 A portion is positioned in the left ventricle LV. The valve leaflet LF is shown as oscillating towards the left atrium LA while the device 14 is below the valve in the left ventricle LV. In this example, the fixation device 14 is similar to the fixation device described above with respect to FIG. 3 and has a proximal element 16 and a distal element 18. The fixation device 14 is at least partially open to extend the distal element 18 radially outward while the proximal element 16 remains held on the shaft 12. It is desirable to engage the leaflet LF with the distal element 18 so that the proximal element 16 is lowered to grip the leaflet LF therebetween.

  One or more flaps 104 may extend radially outward from the catheter 86 as shown and positioned on the atrial side of the leaflet LF. These flaps 104 may be composed of any suitable material such as metal, polymer or fiber and may have any suitable form such as solid, mesh or woven. Further, the flap 104 may have any suitable shape and may have one or more notches 106. As shown in FIG. 9B, the notches 106 may be sized and positioned to allow the proximal element 16 of the fixation device 14 to extend through these notches. As a result, the flap 104 can be held on the atrial side of the valve membrane LF to restrict upward movement or shaking of the valve membrane LF. This positions the leaflet LF for optimal grasping between the proximal and distal elements 16,18. Once the leaflets have been grasped, the flap 104 may be removed with the catheter 86 or may be left behind to help retain the leaflets LF.

  FIGS. 10A-10B illustrate another embodiment of stabilizing the leaflet LF by reducing upward movement or swaying of the valve leaflet LF. As shown in FIG. 10A, the catheter 86 is advanced into the left atrium LA of the heart H, and the fixation device 14 is advanced through the catheter 86 and the mitral valve MV having the leaflet Lf to provide the fixation device. At least a portion of 14 is positioned within the left ventricle LV. The valve leaflet LF is shown as swinging upward toward the left atrium LA while the fixation device 14 is below the valve in the left ventricle LV. In this example, the fixation device 14 is similar to the fixation device described above with respect to FIG. 3 and has a proximal element 16 and a distal element 18. The fixation device 14 is at least partially open to extend the distal element 18 radially outward while the proximal element 16 remains held on the shaft 12. It is desirable to engage the leaflet LF with the distal element 18 so that the proximal element 16 is lowered to grip the leaflet LF therebetween.

  One or more expandable members 110 may extend radially outward from the catheter 86 as shown and positioned on the atrial side of the leaflet LF. The expandable member 110 may be composed of any suitable material such as silicone or polyurethane, and may have any suitable form such as a balloon. FIG. 10B shows an additional view of this embodiment. As shown, the expandable member 110 can be extended in the left atrium and held on the atrial side of the leaflet LF to limit upward movement or swaying of the leaflet LF. This positions the leaflet LF for optimal grasping between the proximal and distal elements 16,18.

  11A-11B illustrate another embodiment that stabilizes the valve leaflet LF by reducing upward movement and swaying of the valve leaflet LF. In this example, the fixation device 14 is similar to the fixation device described above with respect to FIG. 3 and has a proximal element 16 and a distal element 18. The fixation device 14 is also advanced through the catheter and the mitral valve with the leaflet LF to position the distal element 18 of the fixation device 14 in the left valve chamber LV. The fixation device 14 is at least partially open to extend the distal element 18 radially outward while the proximal element 16 remains held on the shaft 12. It is desirable to engage the leaflet LF with the distal element 18 so that the proximal element 16 is lowered to grip the leaflet LF therebetween. However, prior to lowering the proximal element 16, an overtube 121 having a slot 123 is advanced over the shaft 12 and positioned on the atrial side of the leaflet LF, as shown in FIG. 11B. The overtube 121 may be composed of any suitable material such as polyimide, polyethyl ethyl ketone (PEEK®), nylon resin (such as Pebak®) or polyurethane, It may have any suitable dimensions to allow the proximal element 16 to pass through these slots. By holding the leaflet LF by the overtube 121, it is possible to limit the upward movement or swaying of each valve LF and to ensure that the leaflet is correctly positioned before the proximal element 16 is lowered. This positions the leaflet LF for optimal grasping between the proximal and distal elements 16,18. The proximal element 16 may then be released, in which case the proximal element 16 passes through the slot 123 to hold the valve membrane between the proximal and distal elements 16,18. Next, the overtube 121 may be retracted and taken out.

  12A-12B illustrate an embodiment in which the valve leaflets are stabilized by applying tension to the tendon attached to the leaflets. Such stabilization may be desired to reduce the upward movement and sway of the leaflet, or simply to reduce leaflet movement. FIG. 12A shows a heart H having a mitral valve MV with a leaflet LF. The chord CH is shown extending from one of the leaflets LF to the left ventricle LV. There are many chordae, extending from both leaflets to the left ventricle, but chords selected for simplicity are shown. As shown in FIG. 12B, a catheter 120 having an expandable member 122 such as a balloon is advanced to the left ventricle LV, the catheter 120 is positioned, and the expandable member 122 is expanded to tension the chordae CH. Is granted. Although FIG. 12B shows the catheter 120 advanced through the aortic valve AV, the catheter 120 can be passed through any suitable route, including through the mitral valve MV or through the diaphragm S. You may approach the cable CH. By applying tension to the chord CH, the position of the attached leaflet LF is adjusted. Thus, the leaflet LF may be manipulated and repositioned by manipulating the catheter 120 and the expandable member 122, including changing expansion of the expandable member 122. In particular, when the expandable member 122 is pressed against the chord CH in the lateral direction, the leaflet LF is pushed down to restrict upward movement and shaking of the leaflet LF. When the valve membrane LF is disposed at a desired position, the valve membrane LF may be fixed by a fixing device as described with reference to FIG. As a modification, a gripping tool may be used to stretch the chord CH.

  The foregoing embodiments concentrate on the mechanical stabilization of the valve leaflets. Additional embodiments focus on stabilizing the valve leaflets by physiologically slowing the leaflet motion. This can be achieved by slowing the natural heartbeat. In one embodiment shown in FIG. 13, a pacemaker 130 or pulse generator is shown having a pacing lead 132 with an electrode 134 extending to the sinoatrial node SA in the right atrium RA. Pace determination is accomplished when pacemaker 130 sends an electrical impulse through pacing lead 132 to electrode 134, thereby stimulating sinoatrial node SA. This stimulates the right atrium RA to pump blood through the heart H to the right atrium RA. Thus, the use of the pacemaker 130 can regulate the pumping action of the heart and thus the movement of the valve leaflets. FIG. 13 shows the fixation device 14 passed through the leaflet LF of the mitral valve MV. The movement of the leaflet LF may be paced, for example, such that the mitral valve MV remains in systole (closed state) for a longer time to help grasp the leaflet LF with the fixation device 14. Good. Similarly, as shown in FIG. 14, the left atrium LV may be paced directly with a pacing catheter 136 by stimulating the left bundle LB. This can be accomplished by advancing the pacing catheter 136 through the aortic valve AV to the left atrium LV as shown.

III. Gripping Assistance Various devices and techniques are provided to assist in gripping the valve membrane effectively and efficiently. Many of these devices and techniques will be described as an aid to the fixation device described with respect to FIG. However, many features can be used for any suitable gripping and / or securing device. In addition, many such techniques and devices can be used to grasp the valve leaflets or other tissue for any purpose.

  In some situations, one or more leaflets LF are not gripped between the proximal element 16 and the distal element 18 at the desired location. For example, less than a desired amount of the leaflet LF may be grasped. Such a reduced amount of capture may, for example, be less effective in treating blood reflux and / or increase the risk that the leaflet LF will slide out of the fixation device. Once a portion of the leaflet LF is gripped, the position of the leaflet LF may be adjusted, for example, to “pull” the leaflet LF into the shaft 12 of the fixation device 14 or increase the amount of capture. Just move forward. Embodiments for assisting such adjustment are shown in FIGS. 15-17 and 18A-18B.

  FIG. 15 shows an embodiment of a fixation device 14 similar to the fixation device 14 shown in FIG. As shown, the leaflet LF is partially grasped between the proximal element 16 and the distal element 18. In this embodiment, a vacuum line 140 extends through the shaft 12 and is connected to a vacuum source 142. The vacuum line 140 has a distal end 144 that projects into a space 146 between the proximal and distal elements 16, 18. By the operation of the vacuum source 142, suction is applied to the space 146 and the valve membrane LF is drawn inward toward the shaft. Thus, as the leaflet LF is grasped, it can be repositioned within the proximal and distal elements by suction. It will be appreciated that the same vacuum line 140 or additional vacuum lines may provide suction to the valve membrane between other proximal and distal elements. Furthermore, it will be appreciated that a suction force may be applied during the initial grip to assist in the gripping action.

  Similarly, as shown in FIG. 16, another embodiment of a fixation device 14 similar to the fixation device 14 shown in FIG. 3 is shown. In addition, the leaflet LF is partially gripped between the proximal element 16 and the distal element 18. In this embodiment, an auxiliary-gripper channel 150 for passage of an auxiliary-gripper 152 having a jaw 154 extends through the shaft 12 but can be of any type such as atraumatic hooks, clamps or claws. There may be a gripping mechanism. Jaw 154 projects into space 146 between proximal and distal elements 16, 18. The retainer-gripper 152 can be advanced to grasp the leaflet LF with the jaw 154 and retract to pull the leaflet LF inward toward the shaft 12. Thus, the valve membrane LF can be repositioned by manipulating the holding-gripping tool 152. It will be appreciated that the same or additional retainer-gripper 152 may be used to reposition the valve leaf between other proximal and distal elements. Furthermore, it will be appreciated that the holding-gripping tool 152 may be used during the initial grip to assist with the gripping action.

  FIG. 17 shows another embodiment of a fixing device 14 similar to the fixing device 14 shown in FIG. In addition, the leaflet LF is partially gripped between the proximal element 16 and the distal element 18. In this embodiment, a conveyor belt 160 is disposed within each distal element 18 such that the surface of the belt 160 contacts the grasped leaflet LF. The conveyor belt 160 is provided on one or more rollers 162. The rotation of the roller 162 moves the conveyor belt 160, thereby moving the contacted valve membrane LF. For example, clockwise rotation of the roller 162 can pull the leaflet LF inward toward the shaft 12 as shown. Similarly, the counterclockwise rotation of the roller 162 can pull the valve membrane LF outward. Thus, the valve membrane LF can be repositioned by the movement of the conveyor belt 160. It will be appreciated that the conveyor belt 160 disposed within the distal element 18 may function alone or consistently. Further, it will be appreciated that the conveyor belt 160 may be used during the initial grip to assist with the gripping action.

  18A-18B illustrate another embodiment of a fixation device 14 that is similar to the fixation device 14 shown in FIG. 3 and has a proximal element 16 and a distal element 18. In this embodiment, the proximal elements 16 are connected by a bridge 166 that straddles the shaft 12. Referring to FIG. 18B, when the leaflets are grasped between the proximal and distal elements 16, 18, a force is applied to direct the bridge 166 toward the base 69 of the fixation device 14 as indicated by arrow 168. Move. Due to the curvature of the proximal element 16, such movement of the bridge 166 pulls the proximal element 16 inwardly toward the shaft 12 (as indicated by arrow 170), thereby pulling the grasped valve membrane into the shaft. Pull inward toward 12 Similarly, applying a force to move bridge 166 away from base 69 moves proximal element 16 outward. Thus, the leaflet can be repositioned by movement of the bridge 166. It will be appreciated that the bridge 166 may move toward the base 69 as the distal element 18 moves toward the closed position. Alternatively, the proximal element 16 may be attached to a cam or other suitable element such that when the distal element 18 is closed, the proximal element 14 is pulled inward toward the shaft 12. Thus, the proximal element 16 may move while the distal element 18 is stationary, or both the proximal element 16 and the distal element 18 may move relative to each other. Furthermore, it will be appreciated that in some embodiments, the distal element 18 may move while the proximal element 16 is stationary.

  19A to 19C show an embodiment of the fixing device 14 similar to the fixing device 14 shown in FIG. 3, wherein a passage for the preliminary gripper 176 to pass through is provided through the shaft 12 as shown. Show. The pre-gripper 176 has a shaft 178 and a jaw 180 disposed near its distal end, but any type of gripping mechanism such as an atraumatic hook, clamp or nail can be used. May be present. Referring to FIG. 19B, the fixation device 14 is advanced through the mitral valve with an atrial approach as described above so that it is in the atrium. The preliminary gripper 176 is advanced through the shaft 12 and manipulated to grip a portion of one or both of the leaflets LF. The preliminary gripper 176 may be steered by any suitable mechanism, including a pull wire, or the preliminary gripper 176 may be preformed in a desired configuration. Further, the preliminary gripper 176 may be rotated within the shaft 12. To stabilize the leaflet and / or to move the leaflet to the desired orientation, the pre-gripping tool 176 may grip one of the leaflets, or hold both leaflets, eg, in a bonded orientation. Good. Once the valve membrane is satisfactorily oriented, the fixation device 14 may be used to grip the valve membrane LF, as shown in FIG. 19C. Next, the preliminary gripping tool 176 may be released from the valve membrane LF and taken out by extraction through the passage in the shaft 12. As a modification, the pre-gripping tool 176 can be left in place to reinforce the fixation of the valve membrane.

  In other embodiments, the pre-gripper 176 is advanced separately to the tissue and leaflet LF, eg, with different approaches. FIG. 20 shows the fixation device 14 advanced by approaching the atrium and the preliminary gripper 176 advanced by approaching the ventricle. The pre-gripper 176 also has a shaft 178 and a jaw 180 disposed near its distal end 182 but may be any type of grip such as an atraumatic hook, clamp or nail. There may be a mechanism. The preliminary gripper 176 is advanced and manipulated to grip a portion of one or both of the leaflets LF. The preliminary gripper 176 may be steered by any suitable mechanism, including a pull wire, or the preliminary gripper 176 may be preformed in a desired configuration. Further, the preliminary gripper 176 may be rotated. To stabilize the leaflet and / or to move the leaflet to the desired orientation, the pre-gripping tool 176 may grip one of the leaflets, or hold both leaflets, eg, in a bonded orientation. Good. Once the valve membrane is perfectly oriented, the fixation device 14 may be used to grip the valve membrane LF. The fixation device 14 is advanced through the mitral valve with atrial approach so that it is in the atrium. This is typically accomplished by passing at least a portion of the fixation device 14 through the leaflet adjacent to the region of the leaflet gripped by the preliminary gripper 176. Next, the preliminary gripper 176 may be released from the valve membrane LF and removed by extraction. As a modification, the pre-gripping tool 176 can be left in place to reinforce the fixation of the valve membrane. It will be appreciated that in other embodiments, the fixation device 14 is advanced by ventricular approach and the preliminary grasper 176 is advanced by atrial approach.

  21A-21B illustrate an embodiment of a fixation device 14 having two single-sided fixation elements 190 that can be joined by a tether 192. FIG. Each single-sided fixation element 190 is composed of at least one proximal element 16 and distal element 18. In some embodiments, the single-sided fixation element 190 is similar to one-half of the fixation device 14 shown in FIG. FIG. 21A shows a pair of single-sided fixation elements 190, each single-sided fixation element 190 grips the leaflet LF between its proximal element 16 and distal element 18. These anchoring elements 190 may be delivered through the delivery catheter 191 to the leaflet LF, and each element 190 is connected to an elongate delivery device 193 passing through the catheter 191. The fixing elements 190 are also connected to each other by a connecting body 192. Once the anchoring element 190 has satisfactorily gripped the valve membrane LF, the anchoring element 190 can be delivered and removed from the device 193 and the valve membrane LF can be left behind and held in the desired orientation via the tether 192. As a modification, the tether 192 may be shortened or extended in order to draw the fixation elements 190 together and thereby join the leaflets LF. In some embodiments, as shown in FIG. 21B, the tether 192 consists of a resilient element such as a coil or spring that “self-shrinks” when released from the catheter 191. Another means of shortening or extending the tether 192 includes attaching a suture fastener to the tether 192, a preferred embodiment of which is described in US patent application Ser. No. 10/087004 (attorney docket). No. 020489-000500 US). In other embodiments, each single-sided fixation element 190 is attached to an individual tether that extends through the catheter 191. In that case, the individual tethers may be tied together and the fastening elements 190 may be tied together at a desired distance by pushing the knot towards the fastening element 190.

  Thus, the fixation elements 190 may be connected to each other, attached, joined, or joined to hold the leaflet LF in the joined position. It will be appreciated that any number of single-sided fixing elements 190 may be used, some or all of which may be joined by one or more tethers 192. It will further be appreciated that at least one of the single-sided fixation elements 190 may be used to grasp tissue other than the valve leaflet such as chordae to assist in the treatment of the valve. For example, the element 190 may join the leaflet to the leaflet, the leaflet to the papillary muscle, and the leaflet to the chordae. Furthermore, it will be appreciated that the single-sided fixation element 190 may be deployed from both sides of the valve, eg, with an atrial approach and a ventricular approach, and joined across the valve. Thus, in order to cure the backflow into the blood, one single-sided fixing element 190 may be deployed on the front side of the valve and one single-sided fixing element 190 on the back side of the valve, and these elements 190 may then be tightly tied together. .

  FIG. 22 is similar to the fixation device 14 shown in FIG. 3 and shows an embodiment of the fixation device 14 having a proximal element 16 and a distal element 18. However, in this embodiment, the distal element 18 is “self-engaging”. As shown in FIG. 22, the fixation device 14 may be positioned such that the distal element 18 is positioned in the atrium and the proximal element 16 is positioned in the atrium. Instead of engaging the leaflet LF with the distal element 18 and then lowering the proximal element 16 to grip the valve LF between the two elements, first the proximal element 16 is lowered to engage each valve LF. Let The lowering of the proximal element 16 may stabilize the leaflet LF and reduce possible upward movement or swaying of the leaflet LF. The distal element 18 then self-engages or automatically moves towards the closed position to engage the leaflet LF and grip the leaflet LF between the proximal and distal elements 16,18 Can do. Self-engagement can be actuated by a variety of mechanisms, including a mechanism that represents the lowering of the proximal element 16 to a predetermined position and a sensor that senses full engagement of the proximal element 16 with the leaflet LF. Good. It will be appreciated that for the fixation device 14 of FIG. 3 without automatic engagement of the distal element 18, a method of lowering the proximal element 16 prior to engagement of the distal element 18 may be utilized.

  Once the leaflets have been grasped, various features can assist in holding the grasped leaflets in the fixation device. For example, FIG. 23 shows an embodiment of a fixation device 14 that holds the position of the leaflets by aspiration after gripping, particularly during movement of the distal element 18 toward the closed position. In this embodiment, the suction line 200 extends to a suction port 202 located on the engagement surface 50 of the distal element 18. The suction line 200 extends through the fixing device to the vacuum source, similar to the embodiment shown in FIG. Once the distal element 18 has engaged the valve membrane with the engagement surface 50, the suction applied through the suction port 202 helps hold the valve membrane to the engagement surface 50. Such suction may be applied before, during, and / or after any proximal element descent to retain the valve membrane. As mentioned above, such aspiration can be particularly useful for securing the leaflets within the fixation device 14 during movement of the distal element 18 toward the closed position.

  In another example, FIGS. 24A-24B show an embodiment of a fixation device 14 having an extended friction appendage. As previously mentioned, the proximal element 16 optionally has a friction appendage, a friction feature, or a gripping force enhancing element to assist in grasping and / or holding the leaflet. 5B, the friction appendage may comprise a barb 60 having a tapered pointed end extending toward the engagement surface 50. As shown in FIG. FIG. 24A shows the proximal element 16 having an extended barb 206 that is directed toward the engagement surface 50 of the distal element 18. Similarly, FIG. 24B shows a detailed view of the barb 206 of the proximal element 16 of FIG. 24A. As shown, the length L is extended. Such extended barbs 206 may be composed of any suitable material, including rubber, flexible or rigid polymers, or various metals. In a preferred embodiment, the extended barb 206 is atraumatic and the additional length L provides increased surface area to hold the valve membrane with frictional forces.

  FIGS. 25A-25B illustrate an embodiment of a fixation device 14 having a patterned gripping surface 212 to help retain the grasped leaflets within the fixation device 14. A specific example of a patterned gripping surface 212 is shown in FIG. 25A. The surface 212 has a plurality of protrusions 214 that extend outward at an angle. The protrusion may be composed of any suitable material, preferably a flexible material such as silicone, polymer or fiber. The protrusion 214 is tilted in a substantially uniform direction to provide friction against an object moving in the opposite direction. The patterned gripping surface 212 may be applied to any suitable portion of the fixation element 14 such as the proximal element 14 or the engagement surface 50 of the distal element 18. FIG. 25B shows the fixation device 14 having a patterned shaved surface 212 on the covering 210 on the distal element 18. A covering 210 may be present to promote tissue growth. In this embodiment, the covering consists of a biocompatible cloth cover positioned on the distal element 18. Cover 210 may optionally be impregnated or coated with various therapeutic agents, including tissue growth promoters, antibiotics, anticoagulants, blood dilution agents and other agents. As an alternative, or in addition, the covering 210 is constructed of a biodestructible or bioabsorbable material so that the treated tissue grows together and then degrades or is absorbed by the body. Also good.

  It will be appreciated that such a covering 10 may cover the distal element 18 and / or the proximal element 16 of any of the fixation devices 14 described herein. The patterned gripping surface 212 is shown disposed on a cover 210 that covers the engagement surface 50. The protrusion 214 is inclined toward the shaft 12 of the fixing device 14. Thus, the leaflet LF can be drawn toward the shaft 12 in the same direction that the protrusion 214 encounters minimal friction. However, the valve membrane LF moving away from the shaft 12 encounters significant friction from the projection 214 when the projection 214 is engaged to prevent movement of the valve membrane LF. Thus, the patterned gripping surface 212 prevents movement of the leaflets away from the shaft 12 and helps retain the gripped leaflets within the fixation device 14.

  FIGS. 26A-26B illustrate another embodiment of a fixation device 14 having a patterned gripping surface 212 to help hold the gripped leaflets. In this embodiment, the surface 212 has a plurality of protrusions 214 that extend outward at an angle. The protrusion may be composed of any suitable material, preferably a rigid material that can be pierced into and / or through the leaflet. Therefore, the protrusion may be sharp or sharp. The patterned gripping surface 212 may be applied to any suitable portion of the fixation device 14, preferably the engagement surface of the distal element 18. FIG. 26A shows the leaflet grasped by the distal element 18, where the protrusion 214 extends through the leaflet LF to help hold the leaflet LF in place. The leaflet LF may then be grasped between the proximal and distal elements 16, 18 to release the proximal element 16. In some embodiments, the proximal element 16 applies a force to the protrusion 214 such that the protrusion 214 “staples” the leaflet LF to the engagement surface 50, as shown in FIG. 26B. Bend 214 toward the engagement surface 50. As a modification, the protrusion 214 may have a barbed or twisted tip that can similarly act to staple the leaflet LF to the engagement surface 50.

IV. Grasping Evaluation Once a tissue or leaflet has been grasped, it is often desirable to assess the quality of the grasp, such as the amount captured, the orientation of the tissue, and the likelihood that the fixation device will maintain the grasp over time. Thus, various devices and techniques are provided for evaluating grip. It will be appreciated that the evaluation device and technique may be used in combination with the aforementioned fixation devices, or may be used with any suitable gripping and / or fixation device. Further, such evaluation devices and techniques may be used to evaluate the grasping of the valve leaflets or other tissue for any purpose.

  One way to determine grip quality is to visualize the grip by fluoroscopy, ultrasound, echocardiography or other known visualization techniques. Using these techniques, the physician or practitioner can observe the fixation device and the image of the grasped tissue to determine if grasping is desired. The fixation device can be visually distinguished from the surrounding tissue by increasing the visibility of the surrounding tissue, particularly portions of the tissue to be grasped, such as the valve leaflets. Thus, as shown in FIGS. 27A-27B, a substance that enhances visibility can be injected into the leaflet LF before and / or after gripping by the fixation device. Examples of these materials are liquid contrast materials or bioabsorbable polymer beads with air bubbles trapped therein. As shown in FIG. 27A, an infusion catheter 220 having a needle 222 may be advanced to the leaflet LF to inject a substance. An exemplary infusion catheter 220 is described in US Pat. Nos. 6,685,648; 4,578,061; 6,540,725; 6,165,164. FIG. 27B shows the leaflet LF into which the substance 224 has been injected (as shown by the projection) and the other leaflets being injected through the needle 222 of the injection catheter 220.

  As a modification, portions of the fixation device may have increased visibility to identify the fixation device from surrounding tissue. For example, FIG. 28 shows the fixation device 14 with the proximal element 16 and the distal element 18 having enhanced visibility, as shown by projection. Such enhanced visibility can help distinguish the proximal and distal elements 16, 18 from the valve leaflet LF captured therebetween. Further, the practitioner will note that the leaflet edge E is positioned relative to the proximal and distal elements 16, 18, eg, how close the edge E is to the shaft 12 of the fixation element 14. Can be determined. This may indicate the size of the capture. In some embodiments, the surface of the fixation device is roughened, for example by bead spraying, to enhance visibility such as echo brightness. In other embodiments, at least portions of the fixation device 14 have a cover with increased visibility. Such a cover may be composed of a cloth having titanium yarn, spun polyester or other material that provides echo brightness. Alternatively, or in addition, the cover may be stamped or impregnated with a material that provides echo brightness, such as barium sulfate. Alternatively, the visibility of the covering may be enhanced by the bulky appearance of the covering.

  In some embodiments, the fixation device has an ultrasound reception indicator. The ultrasound reception indicator is typically positioned along the proximal or distal element near the target area. This indicator is used to determine the presence or absence of tissue in the target area, thereby determining the quality of the grip. The indicator consists of a chip or other device that resonates or vibrates at a specific ultrasonic frequency that is different from the general frequency used to visualize the remainder of the fixation device and the surrounding tissue. Thus, when a specific ultrasound frequency is used for visualization, the indicator shows a bright visual artifact in the echocardiogram. This indicates that the tissue is not sufficiently grasped in the target area because the indicator is free to vibrate. However, if the tissue is compressed between the proximal and distal elements within the target region, the tissue compresses the indicator to reduce or dampen the indicator vibration. Thus, if no bright visual artifact is seen at a particular ultrasound frequency, it can be determined that the tissue is sufficiently grasped within the target area of the fixation device. This allows the practitioner to positively assess gripping by looking at the dynamic changes in the image being seen when interrogating at a particular ultrasonic frequency.

  Alternatively, the indicator may consist of a chip or other device that resonates at the same general frequency used to visualize the rest of the fixation device and the surrounding tissue. When the general frequency is used for visualization, the indicator shows a bright visual artifact in the echocardiogram. This indicates that the tissue is not sufficiently grasped in the target area because the indicator is free to vibrate. Also, if the tissue is compressed between the proximal and distal elements within the target region, the tissue compresses the indicator to reduce or attenuate the indicator vibration. Thus, if no bright visual artifact is seen at the general ultrasound frequency, it can be determined that the tissue is sufficiently grasped within the target area of the fixation device. Thus, the practitioner can evaluate grasping by looking at a more static echocardiogram. Both of the aforementioned ultrasound reception indicators may be used for real-time ultrasound images, but one of the grips based on viewing the dynamic changes in the image by interrogation at a particular ultrasound frequency. It will be appreciated that the evaluation is performed and the other evaluates gripping based on viewing a more static image at the general ultrasonic frequency.

  In other embodiments, the fixation device has a magnetic indicator. This magnetic indicator is typically located along the proximal or distal element near the target area. This indicator is used to determine the presence or absence of tissue in the target area and thereby assess the quality of the grasp. This indicator consists of a device such as a ball bearing that is movable when a magnetic field is applied. Such a magnetic field may be applied locally, for example by a catheter, or may be applied entirely, for example, by magnetic resonance imaging. The movement of the indicator may be visualized by any suitable medium such as fluorescence projection. Such movement indicates that the tissue is not sufficiently grasped within the target area because the indicator is freely movable. However, if the tissue is compressed between the proximal and distal elements within the target region, the tissue compresses the indicator to reduce or attenuate the movement of the indicator. Thus, if movement is reduced or not seen when a magnetic field is applied, it can be determined that the tissue is sufficiently grasped within the target area of the fixation device. Thereby, the practitioner can positively evaluate gripping.

  In other embodiments, the position of the grasped leaflets within the fixation device may be determined based on the visibility of the friction element. Such friction elements typically have an observable shape such as a barb and are coated or constructed of a high visibility material. FIG. 29 shows the fixation device 14 having a barb 60 disposed on the proximal element 16 as a friction element. In this embodiment, the proximal element 16 has a visually opaque or semi-opaque covering 230 that covers the barb 60. The cover 230 may be composed of, for example, gold fibers coated for sputtering or sputtered or platinum wires or polymer fibers. When the leaflet LF is grasped and captured between the proximal element 16 and the distal element 18, the leaflet LF presses the cover 230 against the proximal element 16 and extends the barb 60 through the cover 230. It can be visually observed by the exposed barb 60 visualization technique. The amount and position of the visible barb indicates the position of the grasped leaflet. For example, when the leaflet LF ′ is gripped and captured between the proximal element 16 ′ and the distal element 18 ′, only a portion of the barb 60 (such as a single barb 60 ′) is exposed. . Thus, the low amount and outward position of the visible barb 60 'indicates that the leaflet LF is not fully captured. In that case, the valve membrane LF may be released and re-gripped.

  In still other embodiments, the position of the grasped leaflets within the fixation device may be determined based on the visible shape of the proximal element 16. In such embodiments, the proximal element 16 may be composed of segment parts separated by a hinge or flexible region 240, as shown in FIG. Proximal element 16 is coated or constructed with a high visibility material. When the leaflet LF is gripped between the proximal element 16 and the distal element 18 and fully captured, the proximal element 16 has a shape that substantially follows the contour of the distal element 18. When the leaflet LF ′ is gripped and partially captured between the proximal element 16 ′ and the distal element 18 ′, the proximal element 16 ′ becomes edge E ′ of the partially captured leaflet LF ′. Can be deflected. Proximal element 16 'may also flex due to various other misorientations of grasped leaflet LF'. Visualization of the shape of the segmented proximal element indicates the location where an irregularity indicating how much of the leaflet has been captured occurs. If the leaflet is not desirably captured, the leaflet LF may be released and regripped.

  In a further embodiment, the position of the grasped leaflet within the fixation device may be determined based on the visibility of the indicator associated with the distal element 18. For example, FIGS. 31A-31B illustrate an embodiment of a fixation device 14 having a distal element 18 with a flap 240. The flap 240 has a mounting end 242 that is attached to the engagement surface 50 or a portion of the distal element 18 and a free end 244 that extends toward the proximal element 16. The flap 240 forms an angle Θ with the engagement surface 5. The flap 240 is coated or configured with a high visibility material so that the practitioner can observe the flap 240 and its angle Θ by visualization techniques. In a preferred embodiment, the distal element 18 is also coated or configured with a high visibility material. Prior to grasping tissue such as the valve leaflet, the flap 240 is fully visible and is positioned at the maximum angle Θ, as shown in FIG. 31A. As the leaflet LF is grasped between the proximal and distal elements 16, 18, the leaflet LF pushes the flap 240 toward the engagement surface 50. When the leaflet LF is fully captured, the leaflet LF may push the flap 240 so that the flap 240 is parallel or identical to the engagement surface 50, as shown in FIG. 31B. Thus, the lack of the flap 240 may be an indicator that the leaflet LF is satisfactorily gripped. As a modification, the practitioner may be able to determine the degree of grasping or capturing based on the angle Θ. For example, a flap 240 having an angle (Θ / 2) may indicate that the leaflet LF only extends halfway along the engagement surface 50. If this is not desired, the leaflet LF may be released and regripped. It will be appreciated that the flap 240 may have any suitable shape, size or position, including a position on the proximal element or any other suitable element. In addition, more than one flap 240 may be present.

  FIGS. 32A-32C illustrate another embodiment in which the position of the grasped leaflets within the fixation device may be determined based on the visibility of the indicator associated with the distal element 18. Here, the indicator consists of a floating block 248 associated with the distal element 18. The floating block 248 is coupled to the distal element 18 to pass through the distal element 18 when force is applied. Block 248 is coated or configured with a highly visible material so that the practitioner can observe block 248 with visualization techniques. In a preferred embodiment, the distal element 18 is also coated or configured with a high visibility material. Typically, the block 248 is spring loaded so that the block 248 is raised toward the proximal element 14 as shown in FIG. 32A prior to grasping tissue such as the leaflets. It is energized. As the leaflet LF is gripped between the proximal and distal elements 16, 18, the leaflet LF presses the block 248 against the engagement surface 50. When the leaflet LF is partially captured as shown in FIG. 32B, a portion of the block 248 may be raised from the engaging surface 50 and visible, and a portion may extend from the opposite side and be visible. May be. The practitioner can determine the position of the leaflet LF based on the rotation position of the block 248. When the leaflet LF is fully captured as shown in FIG. 32C, the leaflet LF can move the block 248 so that it is completely passed through the distal element 18 and extends outwardly from the opposite side. Thus, the practitioner can determine the desirability of gripping based on the position of the floating block 248. It will be appreciated that the block 248 may have any suitable shape, size or position, including a position on the proximal element 16 or any other suitable element. In addition, there may be more than one block 248.

  FIG. 33 shows an embodiment where the indicator comprises a bladder or reservoir 249 associated with the distal element 18. The reservoir 249 is coupled to the distal element 18 to pass through the distal element 18 when force is applied. The reservoir 249 is filled with a highly visible material so that the practitioner can observe the reservoir 249 by visualization techniques. Typically, reservoir 249 is positioned to be raised toward proximal element 14 as shown on the left side of FIG. 33 prior to grasping tissue such as leaflet LF. When the leaflet LF is gripped between the proximal and distal elements 16, 18 as shown on the right side of FIG. 33, the leaflet LF presses the reservoir 249 against the engagement surface 50. When the valve membrane LF is partially captured, a part of the reservoir 249 may be raised from the engagement surface 50 and visible, or a part may extend from the opposite side and be visible. The practitioner can determine the position of the valve membrane LF based on the position of the reservoir 249. When the leaflet LF is fully captured, the leaflet LF can move the reservoir 249 so that it is fully threaded through the distal element 18 and extends outwardly from the opposite side. Thus, the practitioner can determine the desirability of gripping based on the position of the reservoir 249.

Similarly, as shown in FIGS. 34A-34B, reservoir 249 is shown in FIG. 34B when reservoir 249 is properly displaced (indicating that both valve membranes have been satisfactorily gripped). Can be combined together to form a unique size or volume. Thereby, it can be shown to the practitioner that the valve membrane LF is desirably gripped.
It will be appreciated that the reservoir 249 of FIGS. 33 and 34A-34B may have any suitable shape, size or position, including a position on the proximal element 16 or any other suitable element. . Further, more than one reservoir 249 may be present.

  FIG. 35 illustrates an embodiment in which the position of the grasped leaflet within the fixation device can be determined based on the visibility of an indicator associated with the distal element 18. In this case, the indicator consists of one or more loops 251, such as a wire loop associated with the distal element 18. The loops 251 are coupled with the distal element 18 such that they pass through the distal element 18 when a force is applied. These loops 251 are coated or configured with a high visibility material so that the practitioner can observe the loops 251 by visualization techniques. Typically, the loop 251 is spring loaded so that the loop 251 is raised toward the proximal element 14 as shown on the left side of FIG. 35 before grasping tissue such as the leaflet LF. It is energized like this. As the leaflet LF is gripped between the proximal and distal elements 16, 18, the leaflet LF pushes the loop 251 toward the engagement surface 50. When the leaflet LF is fully captured as shown on the right side of FIG. 35, the leaflet LF can move the loop 251 to pass completely through the distal element 18 and extend outward from the opposite side. . Thus, the practitioner can determine the desirability of gripping based on the position of the loop 251. It will be appreciated that the loop 251 may have any suitable shape, size or position, including a position on the proximal element 16 or any other suitable element.

  FIGS. 36A-36B illustrate another embodiment in which the position of the grasped leaflet within the fixation device can be determined based on the visibility of the indicator associated with the distal element 18. In this case, the indicator consists of at least one slack line 265 such as a wire, suture, thread, filament, polymer or strand extending around portions of the fixation device 14. In this embodiment, as shown in FIG. 36A, the slack line 265 extends along the shaft 12 through the lumen in the catheter 86 and toward the base 69 of the fixation device 14. The slack plug 265 then extends around the free end 54 'to one of the distal elements 18' and continues transversely to the free end 54 "of the opposite distal element 18" An indicator segment 265a is created between elements 18 ', 18' '. Loose plug 265 then extends toward base 69 and returns along shaft 12 to another lumen (or the same lumen) in catheter 86. The slack plug 265 is coated or configured with a highly visible material so that the practitioner can observe the slack line 265 by visualization techniques. Also, the slack line 265 has a slack sufficient to allow at least the movement of the indicator segment 265a when force is applied, for example, by a leaflet. FIG. 36B shows the fixation device of FIG. 36A in which a pair of leaflets LF are desirably gripped. In this case, the desired positioning of the leaflets between the proximal element 16 ′, 16 ″ and the distal element 18 ′, 18 ″ causes the indicator segment 265a to be configured differently, in which case the indicator segment 265a is lowered. Thus, the practitioner can determine the desirability of gripping based on the position of the indicator segment 265a. It will be appreciated that the indicator segment 265a and / or the slack line 265 may have any configuration and that one or more slack lines 265 may be present.

  In other embodiments, the location of one or more leaflets LF within the fixation device 14 may be determined or confirmed prior to the proximal element 16 being released. For example, FIG. 37A shows an embodiment of a fixation device 14 that may be shaped similarly to the proximal element, but has a smaller gripper 263 that is smaller in size. Each mini gripper 263 is disposed between a set of proximal and distal elements 16, 18. The fixation device 14 is positioned so that the valve membrane is engaged by the engagement surface 50 of the distal element 18. The small grippers 263 that each extend radially outward from the shaft 12 a short distance along the engagement surface 50 of the distal element 18 are then released. It will be appreciated that the small gripper 263 may be released separately or simultaneously. If the small gripper 263 grips the valve membrane, it can be determined that the valve membrane is properly positioned in the fixation device 14. This is because such gripping indicates that the leaflet extends to a desired distance with respect to the shaft 12. Once the desired grasping of the leaflet is determined, the proximal element 16 can be released and the leaflet can be grasped between the proximal and distal elements 16,18. Small gripper 263 may remain in place or may be removed.

  As a modification, both the small gripper 263 and the proximal element 16 may be deployed simultaneously. The proximal element 16 can then be raised or released while the small gripper 263 remains deployed, so that it can be determined whether the leaflets are still held by the small gripper 263. If the small gripper 263 still holds the valve membrane, it can be determined that the valve membrane is properly positioned within the fixation device 14. This is because such gripping indicates that the leaflet extends to a desired distance with respect to the shaft 12. Once the desired grasping of the leaflets has been determined, the proximal element 16 can be re-released to grasp the leaflets between the proximal and distal elements 16,18. Small gripper 263 may remain in place or may be removed.

  In still other embodiments, as shown in FIG. 37B, if the released mini gripper 263 does not contact the valve membrane in the target area, the mini gripper 263 passes through the window 265 or space in the distal element 18. It may extend. Thus, as shown, the visualization of the small gripper 263 extending beyond the distal element 18 indicates that the leaflets were not desirably gripped. Such visualization may be accomplished before or after the proximal element 16 is released. When the small gripper 263 is released simultaneously with the proximal element 16, such visualization can achieve an assessment of gripping without further movement of the proximal element 16.

  In other embodiments, the position of the grasped leaflets within the fixation device is the visibility of the released material that is visible with a visualization technique such as a liquid contrast material or bioabsorbable polymer bead that has trapped bubbles therein. It may be determined based on sex. In one embodiment shown in FIG. 38A, the substance 258 is contained in a bladder or reservoir 260 within the distal element 18. As the leaflet LF is grasped between the proximal and distal elements 16, 18, the leaflet LF pushes the reservoir 260 and releases material 258 through the port 262 as shown in FIG. The port 262 may be disposed along the length of the distal element 18 such that the substance 258 is expelled through the port 262 only in the region where the leaflet LF is gripped. Thus, the practitioner can determine the degree of grasping or capturing based on the location and / or amount of the expelled material 258. It will be appreciated that the reservoir 260 may have any suitable shape, size or position, including a position on the proximal element 16 or any other suitable element. Further, more than one reservoir 260 may be present.

In other embodiments shown in FIGS. 39A-39B, the position of the grasped valve membrane within the fixation device is also visible with visualization techniques such as liquid contrast material or bioabsorbable polymer beads that have trapped bubbles therein. Is determined based on the visibility of the released material. In this case, the substance 258 is released through a lumen 270 extending through the shaft 12 of the fixation device 14 and a conduit 272, as shown in FIG. 39A. The conduit 272 is directed to the target area of the engagement surface 50 of the distal element 18. The target region is positioned so that the grasped valve membrane LF covering the target region is considered to be sufficiently grasped. When the valve membrane LF covers the target area as shown in FIG. 39A, the released or injected substance 258 is blocked by the valve membrane LF. Such blockage may prevent injection of substance 258, or may cause injection of substance 258 into valve membrane LF, or some of substance 258 on the side of valve membrane LF receiving the injected substance 258. Some degree of visibility may be allowed. Thus, the practitioner is satisfactorily grasped by the deficiency or depletion of the substance 258 or the position of the injected substance 258 (ie, the position within the leaflet or the side of the valve that receives the injected substance 258). Can be judged. As shown in FIG. 39B, if the leaflet LF does not cover the target area, the released or injected substance 258 is not blocked by the leaflet LF. Thus, the substance 258 is injected into the region between the proximal and distal elements 16, 18 and wanders freely into the circulation. Thus, the practitioner can determine that the object 258 is not fully grasped due to the visibility of the interspersed material 258. It will be appreciated that the conduit 272 may have various forms, sizes and orientations and may be directed to various target areas. In addition, there may be more than one conduit 272. It will also be appreciated that a needle, tube or other instrument may be advanced through conduit 272 to deliver a substance or for any other purpose.
It will also be appreciated that the aforementioned lumen 270 and conduit 272 may be used alternately to draw aspiration. When the leaflet LF covers the target area as shown in FIG. 39A, suction drawn through the conduit 272 pushes the leaflet LF against the conduit 272 to prevent blood from entering the conduit 272. However, blood is aspirated through the conduit 272 when the leaflet LF does not cover the target area. Thus, the practitioner can determine that he is gripping satisfactorily based on the presence of blood aspirated through conduit 272.

  Similarly, the embodiment shown in FIGS. 40A-40B having a lumen 270 extending through the shaft 12 of the fixation device 14 and the conduit 272 is shown. Again, the conduit 272 is directed to the target area of the engagement surface 50 of the distal element 18. The target region is positioned so that the grasped valve membrane LF covering the target region is considered to be sufficiently grasped. In this embodiment, probe 280 can be advanced through lumen 270. The probe 280 is connected to the insertion depth gauge 282 so that the practitioner can determine the advance distance of the probe 280. When the leaflet LF covers the target area as shown in FIG. 40A, the probe 280 may only be advanced until it contacts the leaflet LF. Thus, the practitioner can determine that the leaflet LF is satisfactorily gripped by the minimum advance distance indicated by the insertion depth gauge 282. Probe 280 can be further advanced toward distal element 18 when leaflet LF does not cover the target area as shown in FIG. 40B. Thus, the practitioner can determine that the leaflet LF is not sufficiently gripped by the advance distance. It will also be appreciated that the conduit 272 may have various forms, sizes and orientations and may be directed to various target areas. In addition, there may be more than one conduit 272.

  Similarly, a detectable element 281 may extend from the shaft 12 of the fixation device 14 as shown in FIGS. 41A-41F. In FIGS. 41A-41B, the detectable element 281 causes the release of each proximal element 16 to draw the associated detectable element 281 to the target area of the engagement surface 50 of the associated distal element 18. , Coupled to the proximal element 16. Each target region is positioned so that the grasped valve membrane LF covering the target region is considered to be sufficiently grasped. As shown on the left side of FIG. 41A, when the leaflet LF ′ covers its corresponding target area, the detectable element 281 ′ contacts the leaflet LF ′. As shown on the left side of FIG. 41A, when the leaflet LF ″ does not cover its corresponding target region, the detectable element 281 ″ extends a further distance than if the leaflet was not present. You can move forward. The detectable elements 281 ', 281' 'are comprised of a detectable material or coating, such as a material that can be detected by fluoroscopy, conductance or impedance signals. Thus, the practitioner can detect the position of the detectable elements 281 ′, 281 ″ and, as a result, determine whether the leaflet is desirably gripped, as shown in FIG. 41B. . The detectable elements 281 ′, 281 ″ are then released from the proximal element 16 and removed upon removal of the fixation device 14. It will be appreciated that the detectable elements 281 may be individually extendable from the shaft 12 (ie, may not be coupled to the proximal element 16). In other embodiments, the detectable element 281 may form a circuit upon contact with the engagement surface 50 of the associated distal element 18. For example, when the leaflet LF ′ covers its corresponding target area, the detectable element 281 ′ contacts the leaflet LF ′ as shown on the left side of FIG. 41A. Thus, the detectable element 281 'does not contact the engagement surface 50 and the circuit remains open. When the leaflet LF ″ does not cover its corresponding target area as shown on the right side of FIG. 41, the detectable element 281 ″ advances toward the target area and touches the engagement surface to make the circuit Can be completed. The integrity of the circuit can be detected by any suitable device, such as an ohmmeter or ammeter, thereby indicating whether the valve membrane is desirably grasped.

  In FIGS. 41C-41D, each detectable element 281 can be advanced from the shaft 12 toward a target area of the engagement surface 50 of its associated distal element 18. As shown on the left side of FIG. 41C, when the leaflet LF ′ covers its corresponding target area, the detectable element 281 ′ contacts the leaflet LF ′ to produce a first shape. As shown on the right side of FIG. 41C, when the leaflet LF ″ does not cover its corresponding target area, the detectable element 281 ″ advances toward the target area and has a second shape different from the first shape. Can occur. The detectable elements 281 ', 281' 'are comprised of a detectable material or coating, such as a material that can be detected by fluoroscopy or by impedance signals. Therefore, the practitioner can detect the shape of the detectable element 281. When both valve membranes are desirably gripped, both detectable elements 281 ′, 281 ″ form a substantially first shape, as shown in FIG. 41D.

  In FIGS. 41E-41F, a single detectable element 281 can be advanced from the shaft 12 toward the target area of the engagement surface 50 of the distal element 18. As shown on the left side of FIG. 41F, when the leaflet LF ′ covers its corresponding target area, a portion 283 ′ of the detectable element 281 contacts the leaflet LF ′ to produce a first shape. As shown on the right side of FIG. 41F, when the leaflet LF ″ does not cover its corresponding target area, a portion 283 ″ of the detectable element 281 advances toward the target area and differs from the first shape. A second shape is produced. The detectable element 281 is comprised of a detectable material or coating, such as a material that can be detected by fluoroscopy or by an impedance signal. Accordingly, the practitioner can detect the shape of the portions 283 ′, 283 ″ of the detectable element 281. When both valve membranes are desirably grasped, both portions 283 ′, 283 ″ of both detectable elements 281 form a substantially first shape, resulting in a symmetrical shape, as shown in FIG. 41F.

  In some embodiments, the fixation device has one or more sensors to determine the position of the grasped tissue. Typically, the sensor determines the presence or absence of tissue in or near it. For example, FIGS. 42A-42B illustrate a fixation device having at least one sensor 290 disposed on or within the distal element 18. In this embodiment, the sensor 290 is positioned near the shaft 12 to determine whether the grasped leaflet LF is fully inserted into the fixation device 14 or only partially inserted. . As shown in FIG. 42A, the sensor 290 generates a first signal 292 when the leaflet LF is not detected near the sensor 290 (this indicates that the leaflet LF is not fully engaged). As shown in FIG. 42B, when the leaflet LF is fully engaged, the sensor 290 detects the leaflet LF nearby and emits a second signal 294 that is different from the first signal 292. Sensor 90 may be any suitable, such as a conductor, strain gauge, wireless sensor, optical sensor, ultrasonic sensor, infrared sensor, electrical resistance sensor, intravascular ultrasonic sensor (IVUS) or pressure sensor, to name a few examples. It may have various forms. As a modification, the sensor 290 may comprise a resonant sensor that is responsive to magnetic energy in the fixation device 14 to indicate insertion of the valve membrane. For example, if the valve membrane is not fully inserted, magnetic energy may be applied to the fixation device 14 so that the sensor 290 does not resonate or is not activated. It will be appreciated that there may be any number of sensors 290 and these sensors may be located in or within any element, including the proximal element 16. FIG. 43 shows the fixation device 14 having a sensor 290 that extends into the target region between the proximal and distal elements 16, 18.

  44A-44B show the fixation device 14 having sensors 290 ′, 290 ″ positioned on the shaft 12. FIG. In this embodiment, sensors 290 ′, 290 ″ emit ultrasonic signals toward the portion of distal element 18 near shaft 12. In FIG. 44A, the leaflet LF ″ is not detected by the sensor 290 ″. This is because the leaflet LF ″ is not grasped between the corresponding proximal and distal elements 16, 18 and the leaflet LF ″ does not extend into the path of the emitted signal. FIG. 44B shows the fixation device 14 that desirably grips both leaflets LF ′, LF ″ so that both sensors 290 ′, 290 ″ sense the leaflets LF ′, LF ″.

  It will also be appreciated that sensors may be used to effect movement of the fixation device. For example, a sensor in the form of a strain gauge may be placed on each of the distal elements. Engaging the distal element with the leaflet imparts tension to the distal element that can be measured by a strain gauge. Thus, when the strain gauge measures a predetermined amount, the proximal element is automatically lowered and the leaflets can be gripped between them. It will be appreciated that strain gauge measurements may be used to perform a variety of other movements or simply to indicate to the practitioner that such movements are acceptable.

V. Evaluation of fixation Once the amount of tissue grip has been evaluated, it is often desirable to evaluate the amount of tissue fixation. This can be achieved by evaluating the improvement in the medical condition being treated. In the case of valvular fixation, improved blood reflux may be evaluated. It is often desirable to evaluate the fixation before delivering and separating the fixation device from the catheter so that the fixation device is repositioned if the improvement is not satisfactory. Thus, various devices and techniques are provided for assessing fixation before delivering the fixation device and separating it from the catheter. It will be appreciated that these evaluation devices and techniques may be used in combination with the aforementioned fixation devices, or may be used with any suitable gripping and / or fixation device. Furthermore, many of such evaluation devices and techniques may be used to evaluate fixation for any purpose.

  45A-45B illustrate an embodiment of an apparatus and method for simulating the resulting placement and function of the fixation device 14 positioned to grasp the leaflet LF of the mitral valve MV. In this embodiment, the fixation device 14 is delivered by catheter 86 to the mitral valve MV. The fixation device 14 is movably coupled to a shaft 12 that is passed through a catheter 86. A sheath 300 is also provided over the shaft 12 and through the catheter 86 to provide support while the anchoring device 14 is positioned within the valve MV and the leaflet LF is grasped between the proximal and distal elements 16,18. It has been. When the valve membrane LF is satisfactorily grasped, the sheath 300 may be retracted as shown in FIG. 45B. Retraction of the sheath 300 exposes the flexible linkage 302 that extends from the shaft 12 to the catheter 86. According to the flexible link device 302, the fixing device 14 can be freely moved by imitating the behavior of the fixing device 14 after being separated from the shaft 12. The improvement in blood reflux can then be evaluated. If the improvement appears to be unsatisfactory, the sheath 300 may be advanced to support the repositioning of the fixation device 14 over the flexible linkage 302. Upon repositioning, the sheath 300 can be retracted and the valve function can be evaluated again. This may be repeated as many times as desired. If the improvement appears satisfactory, the fixation device 14 may be separated from the shaft 12.

  Similarly, FIGS. 46A-46B also illustrate an apparatus and method embodiment for simulating the resulting placement and function of the fixation device 14 positioned to grasp the leaflet LF of the mitral valve MV. Yes. In this embodiment, the fixation device 14 is delivered by catheter 86 to the mitral valve MV. The fixation device 14 is movably coupled to a shaft 12 that is passed through a catheter 86. Here, the shaft 12 is composed of a flexible structure 306 such as a compression coil held rigidly by a central actuation wire 308. The wire 308 is held to provide support while the fixation device 14 is positioned within the mitral valve MV and the leaflet LF is grasped between the proximal and distal elements 16,18. When the leaflet LF is satisfactorily grasped, the tension of the wire 308 is released to flex the flexible structure 306, thereby imitating the behavior of the fixation device 14 after separation from the shaft 12, and freeing the fixation device 14 Can be moved to. The improvement in blood reflux can then be evaluated. If the improvement appears to be unsatisfactory, tension may be reapplied to the wire 308 to provide support for repositioning of the fixation device 14. Upon repositioning, the tension can be released again and the valve function can be evaluated. This may be repeated as many times as desired. If the improvement appears satisfactory, the fixation device 14 may be separated from the shaft 12.

  In other embodiments, the fixation device 14 can be separated from the shaft while maintaining a tether such as a suture line to the catheter. Thereby, the fixing device is separated from the shaft, but the fixing device 14 can be evaluated while assisting the recovery of the fixing device for repositioning. A tether may exist specifically for this purpose, or other elements used to position the anchoring device 14, such as the locking line 92 or the proximal element line 90, may be used as the tether. Alternatively, the snare may be extended from the catheter 86 to retrieve the fixation device 14. In either case, the fixation device can be retrieved with the tether, recombined with the shaft 12 and repositioned until satisfactory results are achieved.

  Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, various modifications, changes and equivalents may be used, and the foregoing description is defined by the appended claims. It should be apparent that it should not be construed as limiting the scope of the invention as set forth.

It is a figure which shows holding | grip of the valve membrane by a fixing device. FIG. 6 shows reversal of the distal element of the fixation device. It is a figure which shows taking out of a fixing device. FIG. 5 shows a position as an example of a fixation device in a desired orientation relative to the valve membrane. FIG. 5 shows a position as an example of a fixation device in a desired orientation relative to the valve membrane. FIG. 5 shows a position as an example of a fixation device in a desired orientation relative to the valve membrane. FIG. 5 shows a position as an example of a fixation device in a desired orientation relative to the valve membrane. FIG. 5 shows a position as an example of a fixation device in a desired orientation relative to the valve membrane. FIG. 3 shows an embodiment of a fixation device in one position. FIG. 3 shows an embodiment of a fixation device in one position. FIG. 3 shows an embodiment of a fixation device in one position. FIG. 3 shows an embodiment of a fixation device in one position. FIG. 3 shows an embodiment of a fixation device in one position. FIG. 3 shows an embodiment of a fixation device in one position. FIG. 3 shows an embodiment of a fixation device in one position. FIG. 3 shows an embodiment of a fixation device in one position. FIG. 3 shows an embodiment of a fixation device in one position.

FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet.

FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. FIG. 5 shows an embodiment of an apparatus for stabilizing a valve leaflet by reducing upward movement and swaying of the valve leaflet. It is a figure which shows embodiment which stabilizes the valve membrane of a valve | bulb by providing tension | tensile_strength to the chord attached to the valve membrane. It is a figure which shows embodiment which stabilizes the valve membrane of a valve | bulb by providing tension | tensile_strength to the chord attached to the valve membrane. FIG. 6 shows a pacing lead extending to a sinoatrial node that adjusts the movement of the leaflets to help grasp the leaflets. FIG. 6 shows pacing the left ventricle directly with a pacing catheter. It is a figure which shows embodiment of the fixing device which has a vacuum pipe line. It is a figure which shows embodiment of the fixing device which has an auxiliary | assistant holding tool. It is a figure which shows embodiment of the fixing device which has a conveyor belt.

FIG. 10 illustrates an embodiment of a fixation device having a proximal element that is adjustable inward to further draw grasped tissue into the fixation device. FIG. 10 illustrates an embodiment of a fixation device having a proximal element that is adjustable inward to further draw grasped tissue into the fixation device. FIG. 4 shows an embodiment of a fixing device adapted for use with a preliminary gripper. FIG. 4 shows an embodiment of a fixing device adapted for use with a preliminary gripper. FIG. 4 shows an embodiment of a fixing device adapted for use with a preliminary gripper. It is a figure which shows the fixation device advanced by the fixing device advanced by the atrial approach, and the ventricular approach. It is a figure which shows embodiment of the fixing device which has two single-sided fixing elements which can be joined by a connection body. It is a figure which shows embodiment of the fixing device which has two single-sided fixing elements which can be joined by a connection body. FIG. 6 shows an embodiment of a fixation device having a self-engaging distal element. It is a figure which shows embodiment of the fixing device which performs suction | inhalation in order to maintain the position of a valve membrane after holding | grip.

FIG. 6 shows an embodiment of a fixation device having an extended friction appendage. FIG. 6 shows an embodiment of a fixation device having an extended friction appendage. FIG. 3 shows an embodiment of a fixation device having a patterned gripping surface. FIG. 3 shows an embodiment of a fixation device having a patterned gripping surface. FIG. 5 shows an embodiment of a fixation device having a grasping surface that enters and holds the grasped tissue. FIG. 5 shows an embodiment of a fixation device having a grasping surface that enters and holds the grasped tissue. It is a figure which shows injection | pouring to the valve membrane of the substance which improves visibility. It is a figure which shows injection | pouring to the valve membrane of the substance which improves visibility. FIG. 6 shows a fixation device where the proximal and distal elements have high visibility. FIG. 5 shows a fixation device in which the position of the grasped leaflets in the fixation device can be determined based on the visibility of the friction element. FIG. 5 shows a fixation device in which the proximal element is composed of segment portions separated by hinges or flexible regions. FIG. 10 illustrates an embodiment of a fixation device in which the position of grasped tissue within the fixation device is determined based on the visibility of an indicator associated with the distal element. FIG. 10 illustrates an embodiment of a fixation device in which the position of grasped tissue within the fixation device is determined based on the visibility of an indicator associated with the distal element.

FIG. 10 illustrates an embodiment of a fixation device in which the position of grasped tissue within the fixation device is determined based on the visibility of an indicator associated with the distal element. FIG. 10 illustrates an embodiment of a fixation device in which the position of grasped tissue within the fixation device is determined based on the visibility of an indicator associated with the distal element. FIG. 10 illustrates an embodiment of a fixation device in which the position of grasped tissue within the fixation device is determined based on the visibility of an indicator associated with the distal element. FIG. 10 illustrates an embodiment of a fixation device in which the position of grasped tissue within the fixation device is determined based on the visibility of an indicator associated with the distal element. FIG. 10 illustrates an embodiment of a fixation device in which the position of grasped tissue within the fixation device is determined based on the visibility of an indicator associated with the distal element. FIG. 10 illustrates an embodiment of a fixation device in which the position of grasped tissue within the fixation device is determined based on the visibility of an indicator associated with the distal element. FIG. 10 illustrates an embodiment of a fixation device in which the position of grasped tissue within the fixation device is determined based on the visibility of an indicator associated with the distal element. FIG. 10 illustrates an embodiment of a fixation device in which the position of grasped tissue within the fixation device is determined based on the visibility of an indicator associated with the distal element. FIG. 10 illustrates an embodiment of a fixation device in which the position of grasped tissue within the fixation device is determined based on the visibility of an indicator associated with the distal element. It is a figure which shows embodiment of the fixing device which has a small holding tool. It is a figure which shows embodiment of the fixing device which has a small holding tool. FIG. 6 shows an embodiment having a reservoir in the distal element for releasing material. FIG. 6 shows an embodiment having a reservoir in the distal element for releasing material.

FIG. 5 shows an embodiment of a fixation device whose position in the grasped tissue is determined based on the visibility of the substance released from the conduit. FIG. 5 shows an embodiment of a fixation device whose position in the grasped tissue is determined based on the visibility of the substance released from the conduit. FIG. 5 shows an embodiment of a fixation device having a probe coupled with an insertion depth gauge to determine whether tissue is desirably grasped. FIG. 5 shows an embodiment of a fixation device having a probe coupled with an insertion depth gauge to determine whether tissue is desirably grasped. FIG. 10 illustrates an embodiment of a fixation device having a detectable element extending toward an engagement surface to determine whether tissue has been desirably grasped. FIG. 10 illustrates an embodiment of a fixation device having a detectable element extending toward an engagement surface to determine whether tissue has been desirably grasped. FIG. 10 illustrates an embodiment of a fixation device having a detectable element extending toward an engagement surface to determine whether tissue has been desirably grasped. FIG. 10 illustrates an embodiment of a fixation device having a detectable element extending toward an engagement surface to determine whether tissue has been desirably grasped. FIG. 10 illustrates an embodiment of a fixation device having a detectable element extending toward an engagement surface to determine whether tissue has been desirably grasped. FIG. 10 illustrates an embodiment of a fixation device having a detectable element extending toward an engagement surface to determine whether tissue has been desirably grasped.

FIG. 6 shows an embodiment of a fixation device having at least one sensor disposed on or in a distal element. FIG. 6 shows an embodiment of a fixation device having at least one sensor disposed on or in a distal element. FIG. 6 shows an embodiment of a fixation device having a sensor extending into a target region between a proximal element and a distal element. FIG. 5 shows an embodiment of a fixation device having a sensor positioned on a shaft. FIG. 5 shows an embodiment of a fixation device having a sensor positioned on a shaft. FIG. 5 shows a fixation device and method for simulating the resultant placement and function of a fixation device positioned to grasp the mitral valve leaflets. FIG. 5 shows a fixation device and method for simulating the resultant placement and function of a fixation device positioned to grasp the mitral valve leaflets. FIG. 5 shows a fixation device and method for simulating the resultant placement and function of a fixation device positioned to grasp the mitral valve leaflets. FIG. 5 shows a fixation device and method for simulating the resultant placement and function of a fixation device positioned to grasp the mitral valve leaflets.

Claims (1)

A fixation device having at least one proximal element and at least one distal element configured to grasp tissue therebetween,
A catheter having a proximal end, a distal end, and a lumen therethrough, and configured to provide intraluminal advancement through at least a portion of the body to tissue;
A shaft comprising a compression coil removably coupled to the securing device ;
A central actuation wire configured to extend through the compression coil to stiffen the compression coil ;
The shaft is configured to pass through the lumen of the catheter, and at least a portion of the shaft includes tissue grasped between the at least one proximal element and the at least one distal element. during are a system for fixing the tissue of the body in which said flexible der Ru, so as to allow movement of the fixing device relative to said catheter.

Images